Introduction

Melanoma is derived from the aberrant growth of melanocytes and is classified into several subgroups such as cutaneous melanoma (CM), uveal melanoma (UM), and mucosal melanoma (MM), based on its tissue locations(Han et al., 2021). Cutaneous melanoma (CM) is the major subgroup of melanoma. Accumulating evidence has revealed that metabolic reprogramming contributes to the tumorigenesis and progression of melanoma. Owing to its low incidence rate, targeting metabolism might be a promising therapeutic approach for the treatment of melanoma and offers a deeper understanding of its pathobiology(Brunner and Finley, 2022; Faubert et al., 2020). However, melanoma-altered metabolic reprogramming remains poorly understood.

The Warburg effect, also known as aerobic glycolysis, is a part of metabolic reprogramming. It increases lactate levels regardless of oxygen availability in tumor cells, providing cancer cell tumorigenicity, progression, and chemoresistance(Guo et al., 2022). Pyruvate kinase isoform M2 (PKM2) is the key enzyme that irreversibly converts phosphoenolpyruvate (PEP) to pyruvate in the last step of glycolysis (Li et al., 2016; Liu et al., 2021). It is shifted between catalytically inactive dimeric and active tetrameric forms, and the PKM2 dimer predominantly serves as a key glycolytic enzyme that provides advantages for tumor progression due to the Warburg effect(Liu et al., 2017). Post-translational modifications of PKM2, such as FGFR1-mediated Tyr105 phosphorylation and ERK1/2-dependent Ser37 phosphorylation, can promote PKM2 from a tetrameric to dimeric form, accelerating its translocation into the nucleus (Christofk et al., 2008; Li et al., 2016). In the nucleus, PKM2 acts as a protein kinase that phosphorylates STAT3(Chen et al., 2022a; Dhanesha et al., 2022) and Histone H3(Niu et al., 2020). Interestingly, nuclear PKM2 also functions as a coactivator for several transcription factors, such as HIF-1α(Luo et al., 2011; Wang et al., 2014) or Oct4(Yang et al., 2018), by which regulates metabolic gene transcription and promotes tumorigenesis or sustains cancer stem cell populations. Furthermore, HIF-1α is constitutively activated in melanoma under both normal and hypoxic conditions and is accompanied by increased glycolysis(D’Aguanno et al., 2021; Malekan et al., 2021). Therefore, the precise mechanisms underlying PKM2 activity regulation and its function as an HIF-1α coactivator might provide a molecular basis for the melanoma targeted therapy.

The tumor necrosis factor alpha-induced protein 8 (TNFAIP8, TIPE) family is composed of four members: TIPE, TIPE1, TIPE2, and TIPE3(Yang et al., 2022). Accumulating evidence suggests that TIPE is strongly associated with the development of various cancers by affecting cell proliferation, apoptosis, invasion, and metastasis(Goldsmith et al., 2017; Niture et al., 2018). Therefore, TIPE is broadly considered pro-cancerous(Padmavathi et al., 2018). However, we previous revealed that TIPE functions as a tumor suppressor in colitis and colitis-associated colon cancer(Lou et al., 2022), indicating that TIPE might serve a multifarious function in malignancies. Hitherto, the role of TIPE in melanoma remains unclear. In this study, we revealed that TIPE-mediated PKM2 Ser37 phosphorylation accelerates PKM2 translocation from the cytoplasm to the nucleus, thereby elevating its binding ability to HIF-1α and hypoxia response elements (HREs), thus promoting metabolic reprogramming. TIPE-mediated metabolic reprogramming can confer tumorigenesis and stem-like phenomena to melanoma cells. This process represents an important regulator of the TIPE family switching between oxidative phosphorylation and aerobic glycolysis, paving the way for cancer-specific metabolism in response to low-oxygen challenge.

Results

TIPE increases aerobic glycolysis in melanoma cells

To characterize how TIPE performs biological functions in melanoma, we examined its expression levels in melanoma cell lines. The results showed that A375 and A875 cells had relatively higher TIPE expression than G361 and MM96L cells. Therefore, we downregulated TIPE expression in A375 cells and overexpressed TIPE in G361 cells to perform further experiments (Fig.S1). Furthermore, we demonstrated that TIPE promotes melanoma tumorigenesis both in vitro and in vivo(Fig.S2).

Consequently, we performed RNA sequencing analysis by overexpressing TIPE in G361 cells (Fig. 1A) to examine the underlying mechanisms involved in the progression of melanoma. The results revealed that the overexpression of TIPE dramatically promoted glycolysis metabolites and the HIF-1α pathway (Fig. 1B, C). Since metabolic reprogramming, especially aerobic glycolysis, is tightly dependent on the HIF-1α pathway(Baik et al., 2019), we assumed that TIPE promotes melanoma progression might via the regulation of metabolic reprogramming. Therefore, we performed a metabolomic analysis after interfering with TIPE in A375 cells. Interestingly, the results indicated that the aerobic glycolysis pathway, including pyruvate and lactate, was significantly inhibited in melanoma cells after TIPE silencing (Fig. 1D), confirming that TIPE facilitates glycolytic metabolism in melanoma. Consequently, ATPase activity, lactate secretion, and ATP content assays were performed to further confirm TIPE-induced glycolytic changes. The results demonstrated that TIPE decreased ATPase activity and ATP content while promoting lactate production (Fig. 1E-G). Additionally, we measured the extracellular acidification rate (ECAR) after the overexpression or downregulation of TIPE using a Seahorse Bioscience Flux Analyzer. The results also revealed that TIPE promoted glycolysis and glycolytic capacity in melanoma cells (Fig. 1H-K).

Figure 1.

Furthermore, we investigated whether TIPE affected HIF-1α transcriptional activity or its expression levels. The results demonstrated that TIPE increased the expression of HIF-1α at both mRNA and protein levels(Fig. S3). Interestingly, TIPE can dramatically activate the hypoxia response element(HRE) reporter activity, with which HIF-1α is more prone to recognize the specific DNA motif to regulate metabolic gene transcription(Chen et al., 2022b)(Fig. 1L).

Collectively, above results demonstrate that TIPE plays a crucial role in promoting melanoma glycolysis. However, the impact of TIPE on the Warburg effect by regulating HIF-1α activity requires further investigation.

TIPE interacts with PKM2, promotes its dimerization and nuclear import

To further study the functions of TIPE in melanoma, we used the Co-IP/MS method to bait the potential binding partners of TIPE (the candidate interacting proteins of TIPE are listed in Table S1). Interestingly, we found that PKM2, the key enzyme in aerobic glycolysis, might be a new partner of TIPE in melanoma (Fig. 2A) (Fig. S4). Next, we performed Co-IP assays to confirm the interactions between TIPE and PKM2. The results revealed that exogenously overexpressed Flag-tagged PKM2 interacted with exogenously overexpressed HA-tagged TIPE (Fig. 2B, C). Furthermore, endogenous interactions between PKM2 and TIPE were confirmed in the A375 cells (Fig. 2D, E). GST-pull down assays demonstrated that TIPE directly bound to PKM2 in vitro (Fig. 2F). Moreover, we performed Doulink assay to further demonstrate their endogenous interactions. The results also showed that endogenous interactions between TIPE and PKM2 were confirmed in G361 cells (Fig. 2G). Based on these interactions, we identified the binding regions between TIPE and PKM2. We generated four fragments of PKM2, including amino acids 1-390(NA1BA2), 45-390(A1BA2), 1-219(NA1B) and 220-390(A2), based on their structural domains (Fig. 2H). The results showed that except for the A2 domain, the NA1BA2, A1BA2, and NA1B domains of PKM2 were necessary for its interaction with TIPE (Fig. 2I). Finally, the TIPE protein was divided into two fragments, including amino acids 1-100 (M1) and 101-198 (M2). The data showed that the amino acids 1-100(M1) and 101-198(M2) of TIPE interacted with PKM2 (Fig. 2J). Taken together, these data revealed that TIPE interacts with PKM2.

Figure 2.

Since TIPE interacts with PKM2 in melanoma, we determined whether TIPE increases aerobic glycolysis by affecting PKM2 expression or its activity. The results showed that TIPE did not influence the expression of PKM2 at either the mRNA or the protein level (Fig. S5). Intriguingly, we demonstrated that dimeric PKM2 was reduced in TIPE-silenced A375 cells (Fig. 2K) and was increased following TIPE overexpression in G361 cells (Fig. 2L). Normally, a dimeric form of PKM2 with low affinity for its substrate, phosphoenolpyruvate (PEP), and a tetrameric form have a high PEP affinity. Moreover, the dimeric form of PKM2 is more prone to translocation into the nucleus and thus exerts protein kinase activity, which confers the Warburg effect and tumorigenesis(Zhou et al., 2022). Western blot analysis of nuclear and cytosolic fractions from A375 cells revealed that PKM2 primarily resided in the cytoplasm in which TIPE was downregulated. Likewise, the nuclear level of PKM2 was increased after overexpression of TIPE in G361 cells (Fig. 2M). Furthermore, we examined the distribution of PKM2 after TIPE overexpression by using a Thermo Fisher EVOS microscopic analysis. As shown in Fig.2N, PKM2 was predominantly present in the nucleus after TIPE overexpression, and this phenomenon was diminished by the administration of a PKM2 dimer formation suppressor (TEPP-46, 100μM). It has been shown that dimeric PKM2 promotes tumor progression by regulating the Warburg effect(Zhou et al., 2022). Thus, we speculated that TIPE restores the nuclear levels of PKM2 to promote melanoma tumorigenicity via a dimeric PKM2-dependent Warburg effect. TIPE requires PKM2 for transcriptional activation of HIF-1α Accumulating evidence has revealed that tetrameric PKM2 is enzymatically active towards pyruvate and acts as a transcriptional coactivator, while it dissociates into a dimer(Wei et al., 2020). Consequently, the dimeric form of PKM2 becomes a coactivator of HIF-1α to transcriptionally activate glycolytic genes in favor of the Warburg effect (Fig.3A)(Ouyang et al., 2018). As PKM2 and HIF-1α both play important roles in the metabolic reprogramming process, it is reasonable to believe that the interactions between TIPE and these two molecules could affect the glycolysis in melanoma. Thus, we investigated whether TIPE promoted the transcriptional activation of HIF-1α in a PKM2-dependent manner.

Figure 3.

To confirm the effect of TIPE activation on HIF-1α transcriptional activity, we tested the ability of TIPE to activate the HRE reporter activity in HRE-luciferase plasmid transfected HEK-293T cells. Not surprisingly, significant augmentation of HRE promoter activation by TIPE was observed, especially when combined with PKM2 (Fig.3B). Consequently, TIPE activated HRE reporter activity in a dose-dependent manner, and this phenomenon was reversed after PKM2 knockdown, demonstrating that TIPE has critical effects on the activation of HIF-1α transcription in a PKM2-dependent manner (Fig.3C). HIF-1α targeted genes such as LDHA and GLUT1 were also upregulated by TIPE in a dose-dependent manner and were reversed by interfering with PKM2 (Fig.3D, E). Due to PKM2 cooperated with HIF-1α to activate glycolytic genes during the Warburg effect, we used the Duolink method to confirm whether TIPE affects the endogenous interaction between HIF-1α and PKM2. The results showed that the interaction between HIF-1α and PKM2 was decreased by TIPE interference, whereas the interaction was increased when TIPE was overexpressed (Fig.3F, G). More interestingly, TIPE enhanced the PKM2/HIF-1α interaction in the nucleus, further indicating that TIPE induced PKM2 nuclear translocation and thus promoted its interaction with HIF-1α (Fig.3H). In addition, the Co-IP assay revealed that TIPE elevated this interaction in a dose-dependent manner (Fig.3I).

Moreover, we analyzed the correlation between TIPE and hypoxia scores using TCGA dataset. Interestingly, we found that the hypoxia score was significantly related to the expression of TIPE (Fig.3J) (Table S2), and the TIPE higher expression group had a higher hypoxia score than the lower expression group in melanoma (Fig.3K).

Collectively, these results demonstrated that TIPE has critical effects on the transcriptional activation of HIF-1α in a PKM2-dependent manner. TIPE promotes HIF-1α transcriptional activation via PKM2 Ser37 phosphorylation The presence of PKM2 in the nucleus enhances glucose metabolism by regulating HIF-1α(Luo et al., 2011). Our results preliminarily demonstrate that TIPE promotes PKM2 dimerization and nuclear import, thereby increasing HIF-1α transcriptional activation and promoting aerobic glycolysis. Normally, Erk1/2-dependent phosphorylation of PKM2 at serine 37 (Ser37) and FGFR1-dependent phosphorylation of PKM2 at tyrosine 105 (Tyr105)(Li et al., 2016; Zhou et al., 2018) are indicative of its dimerization and translocation, further promoting the Warburg effect and serving as a transcription factor coactivator(Novoyatleva et al., 2019; Wei et al., 2020). As shown in Fig.4A, interference with TIPE in A375 cells blocked PKM2 Ser37 phosphorylation, and overexpression of TIPE in G361 cells caused Ser37 phosphorylation compared to controls. However, the phosphorylation of PKM2 Tyr105 did not show any obvious changes. Consequently, we hypothesized that this transformation caused by Ser37 phosphorylation affects the interaction between TIPE and PKM2. As expected, the mutation of PKM2 at S37A blocked its interaction with TIPE, but not with the Y105D mutation (Fig.4B). Interestingly, this mutation also interfered with the interaction between PKM2 and HIF-1α, which was elevated by TIPE overexpression (Fig.4C). A previous study has revealed that TIPE promotes chemoresistance in acute myeloid leukemia (AML) by activating the ERK signaling pathway(Pang et al., 2020). In addition, phosphorylation of PKM2 at serine 37 is ERK1/2-dependent manner(Yang et al., 2012). TIPE does not serve as a phosphorylase to perform such post-translational modifications directly. Taken together, these results indicate that TIPE promotes PKM2 dimerization depending on ERK signaling. As expected, the ERK inhibitor, U0126, inhibited PKM2 Ser37 phosphorylation induced by TIPE overexpression (Fig.4D). To investigate whether TIPE affects the binding affinity of PKM2 to the Hif-1α specific binding site of the LDHA and GLUT1 promoter using chromatin immunoprecipitation qPCR (ChIP-qPCR) analysis, we found that TIPE increased the binding of PKM2 to the LDHA and GLUT1 promoters. This phenomenon, caused by the overexpression of TIPE, was diminished after the administration of TEPP-46, indicating that TIPE promoted the binding of PKM2 to the LDHA and GLUT1 promoters in a dimeric PKM2-dependent manner (Fig.4E, F). Finally, we demonstrated that the augmentation of TIPE on HRE promoter activation or HIF-1α targeted genes such as LDHA and GLUT1 was blocked by the S37A mutation (Fig.4G-I).

Figure 4.

In brief, we revealed that TIPE promoted HIF-1α transcriptional activation via ERK-dependent PKM2 Ser37 phosphorylation.

TIPE facilitates melanoma tumorigenesis and aerobic glycolysis in a dimeric PKM2-dependent manner

Several studies have demonstrated that dimeric PKM2 increases tumor progression by regulating the Warburg effect. Therefore, we speculated that TIPE promotes melanoma growth through a dimeric PKM2-dependent Warburg effect. To demonstrate this, we knocked down TIPE in A375 cells and found that cell proliferation was decreased. Interestingly, we found that Pyridoxine, a PKM2 dimer formation inducer (Wei et al., 2020), was sufficient to abrogate the TIPE silencing-mediated cell proliferation (Fig.5A). Consistently, TEPP-46, a PKM2 dimer formation suppressor, was sufficient to reverse the increased proliferative capacity induced by TIPE-overexpression in G361 cells (Fig.5B). Clone formation ability (Fig.5C, D) and in vivo experiments (Fig.5E-G) also demonstrated this phenomenon. Interestingly, we found that decreased ECAR, glycolysis, and glycolytic capacity induced by TIPE interference could be fully antagonized by Pyridoxine in A375 cells (Fig.5H-J). In addition, TEPP-46 reversed the ECAR, glycolysis, and glycolytic capacity induced by TIPE overexpression in G361 cells (Fig.5K-M).

Figure 5.

Lastly, to further demonstrate how TIPE affects the PKM2/HIF-1α pathway during the Warburg effect, we revealed that inhibition of PKM2 dimerization can rescue TIPE-induced cell proliferation. However, this phenomenon was diminished by the activation of HIF-1α, demonstrating that TIPE promotes melanoma cell proliferation via dimeric PKM2 dependent HIF-1α activation (Fig.5N, O). More interestingly, we evidenced that suppression of PKM2 dimerization inhibited the TIPE-mediated Warburg effect. In addition, this phenomenon was diminished by the activation of HIF-1α (Fig.5P, Q).

Taken together, these data suggest that TIPE regulates cell growth and the Warburg effect by inducing the formation of dimeric PKM2, and thus activating the HIF-1α pathway.

TIPE accelerates melanoma cells stem-like phenomenon via promoting PKM2 dimerization under normoxic conditions

Increasing evidence has shown that the HIF-1α pathway is associated with acquisition of cancer stem-like properties(Weinstein et al., 2022; Zhu et al., 2022). To confirm the effects of TIPE on the stemness of melanoma cells under normoxic conditions, we examined the stemness-associated features in vitro. First, we measured cancer stem-like phenotype markers, including NANOG, NOTCH, OCT3/4, SOX2 and BMI-1. The results showed that the markers were increased after overexpression of TIPE in G361 cells (Fig.6A) and were reduced after TIPE interference in A375 cells by using qPCR method (Fig.6B). We further revealed that TIPE increased the migration ability and increased sphere formation (Fig.6C, D). In addition, TIPE significantly increased the chemosensitivity of melanoma cell to sorafenib (Fig.6E, F). Next, we examined the tumorigenicity of melanoma cells with TIPE knockdown in vivo by injecting Ctrl-sh or TIPE-sh A375 cells subcutaneously into nude mice at three dilutions (1×10⁶, 1×10⁵ and 1×10⁴) and allowing them to grow for four weeks. The Confidence intervals (CIs) for 1/ (stem cell frequency) using extreme limiting dilution were calculated as previous reported(Hu and Smyth, 2009; Niu et al., 2021). The estimated CI for the frequency of CSCs in the TIPE knockdown group was 202749, compared with 18441 in the control group (P<0.001) (Fig.6G) (Table S3, 4). Moreover, CD44⁺ subpopulations were significantly elevated, as detected using a fluorescence-activated cell sorting (FACS) assay (Fig.6H, I).

Figure 6.

Because TIPE promotes HIF-1α transcriptional activation in a dimeric PKM2-dependent manner, we performed a sphere formation assay by overexpressing TIPE in G361 cells. The results showed that TEPP-46 partially reversed mammosphere formation induced by TIPE overexpression. Moreover, overexpression of HIF-1α diminished this phenomenon, indicating that TIPE-induced sphere formation depended on dimeric PKM2-dependent HIF-1α activation (Fig.6J). In addition, the increased CD44⁺ subpopulations of G361 cells induced by TIPE were decreased by the administration of TEPP-46, and could be rescued by overexpression of HIF-1α(Fig.6K).

These findings strongly suggest that TIPE maintains melanoma cell stemness via dimeric PKM2-dependent HIF-1α activation.

TIPE is positively correlated with the levels of PKM2 Ser37 phosphorylation and cancer stem cell markers

We analyzed the expression of TIPE in melanoma and benign skin tumors, and the results showed that the expression of TIPE was dramatically increased compared to controls using a tissue chip (Fig.7A, B). To determine if there was a correlation between TIPE and PKM2 Ser37 levels, TIPE and PKM2 Ser37 expression was analyzed by IHC staining. The results showed that TIPE expression was positively correlated with PKM2 Ser37 expression (P < 0.001) (Fig.7C, D).

Figure 7.

Consistent with the above findings, immunohistochemistry (IHC) results showed that TIPE, PKM2 Ser37, LDH, and CSCs marker CD44 were inhibited in A375 TIPE-interfering cell-derived xenografts (Fig.7E). Lastly, TCGA dataset revealed that TIPE has a positive relationship with CSCs markers including BMI1, NANOG, NOTCH1, and OCT3/4(POU5F1) in melanoma (Fig.7F-I).

These results further demonstrate that TIPE maintains cancer stem cell phenotypes in a PKM2 dimerization manner.

Discussion

Accumulating evidence has revealed that TIPE serves as an oncogene and a negative regulator of apoptosis. Its overexpression is positively associated with the development of various cancers, including liver, lung, and breast cancers(Lou et al., 2022; Niture et al., 2018). However, Chen et al. reported that TIPE initially inhibits cancer cell proliferation but promotes tumor migration and metastasis(Li et al., 2021). In addition, a previous report has demonstrated that TIPE functions as a tumor suppressor in certain inflammatory carcinogenesis(Lou et al., 2022). These results suggest that TIPE plays a variety of roles in cancer progression. Interestingly, Niture et al. reported that TIPE promotes prostate cancer progression by regulating oxidative phosphorylation and glycolysis(Niture et al., 2021). However, the mechanism through which TIPE regulates metabolic reprogramming remains unclear. Here, we demonstrate that TIPE facilitates the Warberg effect by promoting dimeric PKM2-mediated HIF-1α transactivation in melanoma. Therefore, targeting TIPE may offer a novel therapeutic approach for melanoma treatment.

Mammalian pyruvate kinase consists of four isoforms, M1, M2, L, and R, which are encoded by two distinct genes (PKM and PKLR) (Valentini et al., 2002). Although these isoforms share similar features, only PKM2 exhibits the lowest basal enzymatic activity and is capable of configuration transformation between the tetramer and dimer, meeting differential metabolic demands(Morgan et al., 2013; Puckett et al., 2021). Cancer cells shift towards the preferential expression of the specific isoform of PKM2, especially its dimeric form, and serve as a pivotal metabolic enzyme that promotes the activation of oncogenic pathways in tumors(Icard et al., 2022). Normally, PKM2 enzymatic activity is accurately modulated in a variety of ways, such as post-translational modifications or metabolite binding, to maintain balanced levels in tumor cells(Puckett et al., 2021). Here, we showed that TIPE promoted melanoma tumorigenesis by promoting glycolysis. The results showed that TIPE interacts with PKM2 and may participate in glycolysis. However, TIPE did not influence the expression of PKM2 at either the mRNA or the protein level. Because of the modulation of PKM2 kinetic properties primarily via its dimer and tetramer configurations, we demonstrated that TIPE could promote its dimeric form transformation, increasing PKM2 residing in the nucleus. However, the downstream signaling pathways that are mediated by TIPE in melanoma remain largely unknown.

The nuclear PKM2 routinely serves as a coactivator to transcriptionally activate certain metabolic genes(Cluntun et al., 2017; Zhang et al., 2019). Because TIPE binds PKM2 and transports it into the nucleus, the dimeric form of PKM2 more easily enters the nucleus to become a coactivator of HIF-1α, resulting in the upregulation of HIF-1α targeted genes such as LDHA and, GLUT1. Thus, we elucidate these relationships in the next step. To verify whether TIPE activates HIF-1α transcriptional activity, we found that TIPE significantly increased the activation of the HRE promoter, especially when combined with PKM2. However, this activation was diminished by interfering with PKM2, indicating that TIPE has critical effects on the activation of HIF-1α transcription in a PKM2-dependent manner. Because PKM2 interacts with HIF-1α and potentiates PKM2-mediated HIF-1α transcription, we found that TIPE increased the interaction between HIF-1α and PKM2. In TCGA dataset, the hypoxia score was positively correlated with the mRNA expression of TIPE in melanoma, and the TIPE higher expression group had a higher hypoxia score than the lower expression group.

The mechanisms associated with PKM2 translocation are diverse, the most important of which is Erk1/2-dependent phosphorylation of PKM2 at serine 37 (Ser37) and FGFR1-dependent phosphorylation of PKM2 at tyrosine 105 (Tyr105)(Li et al., 2016; Zhou et al., 2018). Consequently, we demonstrated that TIPE increased the levels of PKM2 Ser37 but not PKM2 Tyr105. Furthermore, we conjectured that this transformation caused by Ser37 phosphorylation affects the interaction between TIPE and PKM2. The results showed that mutation of PKM2 at S37A blocked its interaction with TIPE but not with Y105D. Because phosphorylation of PKM2 at serine 37 is dependent on ERK1/2(Yang et al., 2012) and TIPE promotes AML chemoresistance by activating the ERK signaling pathway(Pang et al., 2020), we used an ERK inhibitor to further demonstrate the activation of HIF-1αinduced by TIPE. Not surprisingly, we found that TIPE facilitates the Warberg effect predominantly by driving PKM2 Ser37 phosphorylation. Furthermore, we demonstrated that the augmentation of TIPE on HRE promoter activation or HIF-1α targeted genes such as LDHA and GLUT1 was blocked by the S37A mutation, as previously reported. These results demonstrated that TIPE promotes HIF-1α transcriptional activation via ERK-dependent PKM2 Ser37 phosphorylation.

Increasing evidence has shown that HIF-1α promotes tumor progression, metastasis, and therapeutic drug resistance by maintaining cancer stemness(Cui et al., 2017; Niu et al., 2021). Here, we observed that TIPE significantly enhanced tumorigenesis, glycolysis, and CSC properties under normoxia in melanoma, whereas suppression of PKM2 dimerization rescued these TIPE-induced effects. Interestingly, we revealed that decreasing of PKM2 dimerization can rescue TIPE induced cell proliferation, glycolysis, and CSC properties. However, this phenomenon was diminished by activation of HIF-1α, demonstrating that TIPE promotes melanoma cells proliferation, glycolysis, and CSC properties via dimeric PKM2 dependent HIF-1α activation. Furthermore, using a tissue ship, we showed that the expression of TIPE in melanoma tissues was dramatically increased compared to that in benign skin tumor tissues. To determine if there was a correlation between TIPE and PKM2 Ser37 levels, the results also demonstrated that TIPE expression was positively correlated with PKM2 Ser37 levels. Consistently, the expression of TIPE has a positive relationship with PKM2 Ser37, LDH, and the CSCs marker CD44 in TIPE-overexpressing cell-derived xenografts. TCGA dataset revealed that TIPE has a positive relationship with CSCs markers, including BMI1, NANOG, NOTCH1, and OCT3/4(POU5F1) in melanoma. These results further demonstrate that TIPE maintains melanoma cell stem phenotypes in a PKM2 dimerization manner.

In summary, we identified that TIPE serves as an oncogenic candidate for melanoma and determined that TIPE promotes the Warburg effect and maintains the stemness of melanoma. TIPE binds to PKM2, inducing its dimeric transformation by enhancing ERK-dependent PKM2 Ser37 phosphorylation, and thus activating the transcription of HIF-1α, providing tumorigenicity and cancer stem-like phenomena for melanoma progression. The newly identified TIPE/PKM2/HIF-1α axis is an ideal therapeutic target for melanoma and opens an avenue for the development of a novel strategy for precision therapy.

Materials and methods

Cell culture and plasmids construction

Human A375, A875, G361, MM96L and HEK-293T cell lines were purchased from the Shanghai Institute of Cell Biology (Chinese Academy of Sciences, Shanghai, China) and were maintained in Dulbecco’s modified Eagle’s medium (DMEM, Gibco) supplemented with 10% fetal bovine serum (FBS, Gibco) at 37°C under 5% CO₂. The TIPE overexpression lentiviral vector (TIPE), TIPE expression knockdown vector (TIPE-sh) and their control vectors were constructed by GeneChem company (Shanghai, China). HIF-1α, PKM2-Flag, TIPE-HA and their truncated vectors were constructed in our laboratory. The mutant vectors such as PKM2 S37A were synthesized by Tsingke Biology Co., Ltd.(Beijing, China). All plasmids were transfected into the cells according to the manufacturer’s protocol.

Cell proliferation, cell cycle and colony formation assays

Cell proliferation was measured using the Cell Counting Kit-8 method (Dojindo, Shanghai, China). For the cell cycle assay, the cells were stained with propidium iodide (PI; Sigma, USA) and were measured with a flow cytometer (FACS Aria 2, BD, USA). For the colony formation assay, cells were seeded, fixed and stained as previously described(Yang et al., 2022).

Transwell assay

Tranwell assay was performed as we previous described(Yang et al., 2022). Photographs of at least three randomly selected fields were captured and were counted.

Bioinformatics, transcriptomics and metabolomics analyses

The correlations between TIPE and HIF1A, Hypoxia score, cancer stem cells (CSCs) markers including BMI1, NANOG, NOTCH1 and OCT3/4(POU5F1) were estimated by using the ASSISTANT for Clinical Bioinformation website (https://www.aclbi.com/static/index.html#/). Transcriptomics and metabolomics were performed and analyzed by GeneChem company (Shanghai, China). Overexpression of TIPE into G361 cells, interfering TIPE in A375 cells and their control group were randomly divided into three groups to perform transcriptomic analyses, respectively. Interfering TIPE in A375 cells and its control group were randomly divided into six groups to perform metabolomic analyses.

ATP content, ATPase activity, pyruvate kinase activity and lactic acid content measurement

The concentration of ATP was determined 72h after overexpression or interfering of TIPE by using an ATP assay kit (Beyotime, S0026) according to the manufacturer’s instructions. ATPase activity was measured by using an ATPase Assay Kit (Sigma-Aldrich, MAK113). Pyruvate kinase activity and lactate production after overexpression or interfering of TIPE were measured using a Pyruvate Kinase Activity Assay Kit (Nanjing Jiancheng, A076-1-1) and Lactic Acid Assay Kit (Nanjing Jiancheng, A019-2-1) according to the manufacturer’s instruction, respectively.

ECAR

The Extra Cellular Acidification Rate (ECAR) of melanoma cells were determined using the Seahorse XF extracellular flux analyzer (Agilent, Santa Clara, CA, USA). The cells were plated, washed before analysis. The cells were then treated at specific time points: glucose (10 mM), followed by oligomycin (1 μM) and 2-DG (50 mM). Finally, the ECAR were measured by the Seahorse XF software.

Chromatin Immunoprecipitation (ChIP) Quantitative PCR (ChIP-qPCR)

Melanoma cells were cross-linked with 1% formaldehyde, lysed with sodium dodecyl sulfate buffer and sonicated. Sheared DNA was immunoprecipitated with PKM2 antibody and negative control anti-IgG, and quantified using SYBR Green Realtime PCR analysis (ABI, USA). Primer sequences are listed in Table S5. Fold enrichment was calculated based on Ct as 2^−Δ(ΔCt), where ΔCt = Ct_IP - Ct_Input and Δ(ΔCt) = ΔCt_antibody - ΔCt_IgG.

Sphere formation assay

Melanoma cells transfected with TIPE or TIPE-sh were plated onto 24-well low attachment surface polystyrene plates (Corning, USA). Cells were grown in DMEM/F12 medium (Invitrogen, USA) for approximately 10 days supplemented with 20ng/mL EGF (Bioworld, BK0026), 2% B27 (Invitrogen, 17504044), 20 ng/mL basic FGF (PeproThech, #100-18B), and 1% N2(Invitrogen, 17502048).

Luciferase reporter assay

Human HEK-293T cells were seeded onto 48-well plates and transiently transfected with pHRE-Firefly luciferase reporter, TIPE-HA and PKM2-Flag or sh-RNA vector targeting PKM2 plasmids together with internal control reporter pTK (Thymidine kinase)-Renilla luciferase by Lipofectamine™ 2000 reagent (Thermo, USA). FLuc and RLuc activities were determined using the Dual-Luciferase Assay System (Promega, USA).

qPCR

mRNA was isolated and cDNAs were synthesized by using a Prime Script RT Reagent Kit (TaKaRa, China) according to manufacturer’s instruction. qPCR was performed using Real SYBR Mixture (CoWin Bioscience, China) on an ABI PRISM 7500 instrument (ThermoFisher, USA). The sequences of the primers used in this study are listed in Table S5.

Duolink proximity ligation assay (PLA)

Duolink® In Situ PLA® kit (Sigma-Aldrich, DUO92101) was performed to demonstrate the endogenous interactions between TIPE and PKM2, and to interpret how TIPE impact the interactions between HIF-1α and PKM2 according to we described previously(Yang et al., 2022; Zhao et al., 2019). Quantification analysis was performed using the ImageJ software.

Nuclear and cytosolic fractionation

Nuclear and cytosolic fractions were prepared using NE-PER Extraction Reagents (Thermo, 78833) according to the manufacturer’s recommendation. Finally, both cytosolic and nuclear subfractions were stored in -80°C prior to western blot.

Western blot

The prepared lysates were separated by 10% sodium dodecyl sulfate polyacrylamide gel electrophoresis and transferred onto PVDF membranes (Bio-Rad, USA). The membranes were then blocked and incubated overnight at 4°C with the primary antibodies (as listed in Table S6). After incubated with secondary antibodies, the protein bands were visualized using a Tanon 5200 Imager (Shanghai, China).

Immunohistochemical and immunofluorescence

Melanoma tissue chip was purchased from Zhongke Guanghua (Xi’an, China) Intelligent Biotechnology Co., Ltd.(#K063Me01), and the clinicopathological characteristics of melanoma specimens are summarized in Table S7. Immunohistochemistry (IHC) staining was performed as previously reported. The samples were finally analyzed by using semiquantitative scoring criteria. The staining index values (0-12) were obtained and calculated(Yang et al., 2022). For immunofluorescence, cells were seeded onto 24-well plates at a density of 5,000 cells per well. Then, the cells were fixed using 4% formaldehyde solution and permeabilized with 0.5% Triton X-100 solution. Finally, cells were incubated overnight with antibodies prior to blocked with 1% bovine serum albumin (BSA) in phosphate-buffered saline containing 0.2% Tween-20. The fluorescence images of the cells were acquired with a fluorescence microscope equipped with appropriate filter combinations.

Co-immunoprecipitation (Co-IP) and Co-immunoprecipitation mass spectrometry (Co-IP/MS)

For Co-IP, the cells were seeded, harvested, and were then washed twice with PBS and digested and lysed in lysis buffer. The lysed supernatant was incubated with Tag-conjugated beads to bait the potential interacted proteins according to the manufacturer’s instruction. For Co-IP/MS, the beads consequently were washed, eluted, resolved, and then stained with Coomassie brilliant blue. The bands were excised and digested with chymotrypsin and subjected to LC-MS/MS sequencing and data analysis by OBiO Technology Corp.,Ltd. (Shanghai, China).

Flow Cytometry Analysis

Cell apoptosis was measured by using a Cell Apoptosis Analysis Kit (Engreen Biosystem Co, Ltd., Beijing, China). The cells were then incubated in serum-free medium for starvation prior to analysis and fixed using 70% ethanol for 12 h. Consequently, cells were washed, incubated with propidium iodide, and analyzed by a FACS scanner (Aria II, BD, USA). For CD44 analyzing, the cells were seeded, harvested, and incubated with anti-CD44 fluorescent antibody. Isotype-matched human immunoglobulins served as controls. Finally, the cells were counted with the FACS scanner.

Mouse xenograft tumor study

Xenograft tumor studies were conducted utilizing the 6-week-old male BALB/c nude mice purchased from the Shanghai SLAC Laboratory Animal Co., Ltd.. The total number of mice was randomly divided into respective groups and maintained in a standard pathogen free environment. All the animal experiments were approved by the Animal Ethics Committee of Zibo Central Hospital, Binzhou Medical University. Tumor growth was monitored regularly and the length, width, and height measurements taken every 7 days. All mice were killed by 10 weeks post injection. For the rescue test, one week after injection, mice bearing TIPE-vector were treated with TEPP-46. TEPP-46 (50mg/kg) or vehicle control (0.9% NaCl) was administrated via intraperitoneal injection. At the end of experiment, mice were euthanized and tumors were collected. Tumors were fixed with 4% paraformaldehyde for further immunohistochemistry (IHC) analysis.

Statistical analysis

GraphPad Prism (GraphPad Software, San Diego, CA) was used for statistical analyses. Two-tailed Student’s t-tests were used to compare two groups. Linear regression analysis was explored to analyze the correlation of TIPE with other indicators. All the data are shown as the mean with standard deviations (SD) from at least three independent experiments. A P value of <0.05 was considered statistically significant for all tests.

Data availability Statement

All the data needed to evaluate the conclusions of the study are presented in this paper. Additional data related to this study may be requested from the corresponding author.

Acknowledgements

This work was supported by the National Natural Science Foundation of China (Nos. 81972002, 12304241, 81971491), Natural Science Foundation of Shandong Province (ZR2023QC68, ZR2023MC136, ZR2021MC083, ZR2021MC165), Medicine and Health Science Technology Development Projects of Shandong Province (202102050803 and 2018WS534), and Qingdao Postdoctoral Application Innovation Project (QDBSH20230102068).

Ethics approval

This study has been approved by the Medical Ethics Committee, the Animal Care and Use Committee of Zibo Central Hospital, Binzhou Medical University.

Author contributions

Peiqing Zhao: Conceptualization, Supervision. Jianxin Du: Methodology, Writing-Original draft preparation. Maojin Tian: Data curation, Investigation. Le Yang: Investigation. Ziqian Zhao: Investigation. Jigang Li: Validation. Qingqing Yin: Software. Lianqing Wang: Data curation. Wei Hu: Investigation. Yunwei Lou: Visualization.

Declaration of competing interest

The authors declare that they have no conflicts of interest concerning this article.