Open Access

Stromal-epithelial lactate shuttle induced by tumor‑derived interleukin‑1β promotes cell proliferation in oral squamous cell carcinoma

  • Authors:
    • Jie Wu
    • Yun Hong
    • Tong Wu
    • Juan Wang
    • Xiaobing Chen
    • Zhi Wang
    • Bin Cheng
    • Juan Xia
  • View Affiliations

  • Published online on: November 17, 2017
  • Pages:687-696
  • Copyright: © Wu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Stromal-epithelial lactate shuttle is an essential process to support fast‑growing tumor cells, however, the underlying mechanism remains ambiguous. Interleukin‑1β (IL‑1β), which is a key node gene in both stromal and epithelial cells of oral squamous cell carcinoma (OSCC), may participate in this metabolic reprogramming. In the present study, anaerobic glycolysis of cancer‑associated fibroblasts (CAFs) was evaluated and the role of IL‑1β in regulating stromal‑epithelial lactate shuttle was determined. A co‑culture system of primary fibroblasts and OSCC cell lines (CAL27, UM1 or SCC25) was created to investigate the stromal‑epithelial interaction. α‑smooth muscle actin (α‑SMA) expression of fibroblasts, IL‑1β expression and cell proliferation of OSCC cells, and a series of glycolytic genes were measured. Recombinant IL‑1β treatment and IL‑1β knockdown in UM1 cells were also used to evaluate the effect of IL‑1β. Expression of α‑SMA, glucose transporter 1, hexokinase 2, lactic dehydrogenase and mono‑carboxylate transporter (MCT) 4 were significantly overexpressed in activated fibroblasts, while IL‑1β and MCT1 were upregulated in OSCC cells, indicating enhanced glycolysis in cells of the tumor stroma and a lactate shuttle to the tumor cells. Furthermore, exogenous IL‑1β induced fibroblasts to present similar expression profiles as that in the co‑culture system. Silencing of IL‑1β significantly abrogated the regulatory effect of UM1 cells on stromal glycolysis. Additionally, carboxy‑fluorescein succinimidyl ester cell tracing indicated that OSCC cell proliferation was accelerated during co‑cultivation with fibroblasts. These results indicate that tumor‑derived IL‑1β enhanced stromal glycolysis and induced one‑way lactate flow from the tumor mesenchyme to transformed epithelium, which promotes OSCC proliferation.


Rapidly growing tumors have large energy demands, but the insufficient nascent vasculature fails to provide sufficient nutrition and metabolic substrates for malignant progression. Thus, cancer cells induce adjacent activated fibroblasts to increase lactate production via the glycolysis pathway. Subsequently, the cancer cells use metabolic intermediates release from fibroblasts to 'fuel' tumor growth (1,2). This reciprocal metabolic reprogramming between cancer cells and the surrounding stroma has been widely recognized as a 'reverse Warburg effect' (3). As the most common metabolic intermediate of glycolysis, lactate is transported via unidirectional mono-carboxylate transporters (MCTs). This 'lactate shuttle' was first reported between astroglial cells and neurons through MCT1 and MCT2 transporters, respectively (4,5). In the tumor microenvironment (TME), MCTs control the lactate exchange between glycolytic and oxidative cancer cells, and between stromal and epithelial cells (5). In the past decade, research has revealed a one-way flow of lactate shuttling from tumor mesenchyme to epithelium (6). This lactate fluxion has essential roles not in adjusting intracellular acid-base balance (7,8), and also providing metabolic fuel for cancer cells.

Oral squamous cell carcinoma (OSCC) is the most common oral malignancy with poor 5-year survival rate (9). Components of the tumor stroma, particularly cancer-associated fibroblasts (CAFs), may be partially responsible for the unfavorable therapeutic results and poor prognosis of OSCC. This raises the questions, is the 'reverse Warburg effect' involved in OSCC progression? Does the stromal-epithelial lactate shuttle 'fuel' oral cancer growth? In our previous study, bioinformatics network construction identified interleukin-1β (IL-1β) as one of the key node genes in the TME during oral carcinogenesis (10). Is this tumor derived-IL-1β a major contributing factor for the lactate flux to cancer cells?

In this study, it was aimed to investigate the function of cancer cell-derived IL-1β on reciprocal metabolic reprogramming between the epithelium and mesenchyme. Thus, a co-culture system was created using OSCC cells and separated fibroblasts from patients or healthy volunteers, and the results revealed that interactions between stromal and epithelial cells upregulated IL-1β expression in tumor cells, which enhanced glycolysis and lactate release in CAFs, which subsequently resulted in accelerated malignant cell proliferation.

Materials and methods

Cell lines

UM1, SCC25 and CAL27 human OSCC cell lines and normal oral keratinocyte (NOK) were used in this study. SCC25 and CAL27 were purchased from American Type Culture Collection (Manassas, VA, USA). OSCC cell line UM1 and NOK were provided by Professor J. Silvio Gutkind (University of California, San Diego, CA, USA). UM1, SCC25 and CAL27 were maintained in Dulbecco's modified Eagle's medium (DMEM; Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) containing 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc.). NOK cells were maintained in Keratinocyte-SFM (Gibco; Thermo Fisher Scientific, Inc.). Cells were incubated at 37°C in 5% CO2. This study was approved by the Ethical Review Committee of Guanghua School of Stomatology, Hospital of Stomatology, Institute of Stomatological Research, Sun Yat-sen University (Guangzhou, China; approval no. ERC-2012-15). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. And all participants provided written informed consent to take part in the study.

Sample selection and primary cell culture

Fibroblasts separated from patients with OSCC, patients with oral leukoplakia and healthy volunteers, were termed CAFs (n=8), Dysplasia-fs (n=8) and normal fibroblasts (NFs; n=10), respectively. All samples were obtained from Department of Oral and Maxillofacial Surgery, Guanghua School of Stomatology, Sun Yat-sen University between February 2014 and September 2015. All patients provided written informed consent to participate in this study. Samples were cautiously washed with phosphate-buffered saline and then digested with 0.2% neutral protease Dispase II (Roche Diagnostics GmbH, Mannheim, Germany) overnight at 4°C. The stromal layer was carefully split from the epithelial layer and shredded into tiny fragments. The fragments were digested with 0.25% trypsin-EDTA (Gibco; Thermo Fisher Scientific, Inc.) at 37°C for 1 min. Following neutralization, centrifugation (at 120 × g for 5 min) and re-suspension at room temperature (RT), fragments were seeded into flasks and incubated in primary culture medium (DMEM containing penicillin, streptomycin and 20% FBS) at 37°C for ~14 days. Subsequently, the fibroblasts were sub-cultured and purified according to the 'adherent time lag' between fibroblasts and epithelial cells. Fibroblasts between passage 4 and 10 (P4-P10) were used.

Co-culture system and fibroblasts activation

OSCC cells and fibroblasts were seeded onto the insert or the bottom well of co-culture Transwell inserts (Corning Incorporated, Corning, NY, USA), respectively, and independently cultured until the cells adhered. The co-culture durations are slightly different between the experiments, and the specific time has been noted in each figure. Once adhered, the insert was placed back into the well for co-culture.

Immunofluorescence (IF) staining

Cells were fixed with pre-cooled 100% methanol for 20 min at −20°C, following permeabilizing [using 0.1% Tween-20 and 1% bovine serum albumin (BSA; Beyotime Biotechnology, Shanghai, China)] for 10 min at RT and antigen blocking for 30 min ar RT, cells were successively incubated with mouse monoclonal anti-α-smooth muscle actin (α-SMA; cat. no. ab7817; Abcam, Cambridge, MA, USA; diluted 1:200) at 4°C overnight, secondary antibody H&L DyLight® 488 (cat. no. ab96875; Abcam; diluted 1:200) at RT for 1 h, and 100 ng/ ml DAPI (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) at RT for 5 min. Images were acquired with a confocal microscope (Carl Zeiss AG, Oberkochen, Germany).

Glucose uptake and lactate assays

The conditioned media (CM) was harvested and stored at −80°C. Glucose and lactate content were measured with a glucose assay kit (Applygen Technologies, Inc., Beijing, China) and lactate assay kit (Nanjing KeyGen Biotech, Co., Ltd., Nanjing, China), respectively, according to the manufacturers' protocols. Absorbance values of test groups were normalized against protein concentrations (n=3).

IL-1β ELISA assay

CM from NOK and OSCC cell lines was harvested after 48 h incubation. IL-1β was measured with ELISA kit (cat. no. SEA563Hu; Cloud-Clone Corp., Katy, TX, USA) according to the manufacturer's protocol. The values were normalized to the cell count (n=3).

Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)

Total RNA was extracted using TRIzol reagent (Thermo Fisher Scientific, Inc.) and then reverse transcribed using qScript cDNA synthesis kit (Roche Diagnostics GmbH). All of the primers were produced by Takara Biotechnology Co., Ltd. (Dalian, China; Table I). qPCR was performed using the the LightCycler® 480 SYBR-Green I Master and the LightCycler® 480 instrument (Roche Diagnostics GmbH). PCR was carried out at 95°C (10 min) and 45 cycles at 95°C (10 sec), 65°C (15 sec) and 72°C (15 sec). Each step was performed according to the manufacturers' protocols. The amounts of target genes were normalized to GAPDH using 2−ΔΔCq calculations (11).

Table I

Primer nucleotide sequences.

Table I

Primer nucleotide sequences.

GenePrimer nucleotide sequences (5′ to 3′)Product size (bp)

[i] GLUT1, glucose transporter 1; HK2, hexokinase 2; PFKM, phosphofructokinase, muscle; PKM2, pyruvate kinase M2; LDHA, lactate dehydrogenase; MCT, mono-carboxylate transporter; IL-1β, interleukin-1β; F, forward; R, reverse.

Western blotting

Cells were harvested and lysed in radioimmunoprecipitation assay buffer and measured with bicinchoninic acid protein assay kit (both from Sigma-Aldrich: Merck KGaA). Then samples (30 mg/lane) were separated by 10% SDS-PAGE and transferred to a polyvinylidene difluoride membrane. Following antigen blocking in 5% nonfat milk for 1 h at RT, the membrane was incubated with primary antibodies overnight at 4°C. The following primary antibodies were used: Rabbit monoclonal anti-α-tubulin (cat. no. 2125; diluted 1:1,000), anti-GAPDH (cat. no. 2118; diluted 1:1,000), anti-hexokinase 2 (HK2) (cat. no. 2867; diluted 1:1,000), anti-lactate dehydrogenase (LDHA; cat. no. 3582; diluted 1:1,000) and anti-IL-1β (cat. no. 12703; diluted 1:1,000) all from Cell Signaling Technology, Inc. (Danvers, MA, USA); mouse monoclonal anti-MCT1 (cat. no. sc-365501; diluted 1:200) and rabbit polyclonal anti-MCT4 (cat. no. sc-50329; diluted 1:400) from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA); mouse monoclonal anti-glucose transporter 1 (GLUT1) (cat. no. 202921; diluted 1:250) from R&D Systems, Inc. (Minneapolis, MN, USA). The membrane was then washed three times with TBS-Tween, and incubated with secondary antibodies goat anti-rabbit IgG (cat. no. 7074; diluted 1:2,000) or horse anti-mouse IgG (cat. no. 7076; diluted 1:2,000) both from Cell Signaling Technology, Inc. for 1 h at RT, according to the source of primary antibodies. The immune-reactive bands were visualized with an enhanced chemiluminescence system (EMD Millipore, Billerica, MA, USA). Band intensities were semi-quantitated using ImageJ software (National Institutes of Health).

Small interfering RNA (siRNA)-mediated downregulation of IL-1β

IL-1β siRNA (si-IL-1β) was designed by and purchased from Invitrogen (Thermo Fisher Scientific, Inc.). Cells were transfected with siRNA pool (including the following sequences: IL-1β-siR NA1 for ward, 5′-GCUCGCCAGUGAAAUGAUGGCUUAU-3′ and reverse, 5′-AUAAGCCAUCAUUUCACUGGCGAGC-3′; IL-1β-siRNA2 forward, 5′-GGAUGACUUGUUCUUUGAAGCUGAU-3′ and reverse 5′-AUCAGCUUCAAAGAACAAGUCAUCC-3′; IL-1β-siRNA3 forward, 5′-GGAUAUAACUGACUUCACCAUGCAA-3′ and reverse 5′-UUGCAUGGUGAAGUCAGUUAUAUCC-3′) or Stealth RNAi® negative control (cat. no. 12935200) by Lipofectamine® RNAiMAX reagent (Invitrogen; Thermo Fisher Scientific, Inc.). UM1 cells (1×106/ml) were cultured in 6-well plates with DMEM containing 10% FBS for 24 h and maintained in a 37°C incubator under a humidified atmosphere containing 5% CO2 (until the density of the transfected cells reached 30–80%). The siRNA or negative control were transfected into the cells using Lipofectamine® RNAiMAX at 10 nM according to the manufacturer's instructions. The transfection efficiency was confirmed by RT-qPCR and western blot analysis (data not shown).

Proliferation assay with carboxy-fluorescein succinimidyl ester (CFSE)

On the basis that CFSE cell fluorescence progressively decreases as cells divide, UM1 cell proliferation was determined using CFSE. Cells were re-suspended in 1 µM CellTrace™ CFSE staining solution (Invitrogen; Thermo Fisher Scientific, Inc.), and incubated at 37°C for 20 min, protected from light. Then 5 times the original staining volume of complete culture medium was added to the cells and the mixture as incubated at 37°C for a further 5 min to terminate the staining reaction. Following three washes with culture media, UM1 cells were co-cultured with fibroblasts for 72 h or cultured alone as the control. UM1 cells were detached from the plates and fixed with 4% paraformaldehyde at 24 h intervals at RT. Subsequently, the CFSE fluorescence was detected by flow cytometry (Beckman Coulter, Inc., Brea, CA, USA) with an excitation light of 488 nm. Results were expressed as a proliferation index (mean level of cell divisions frequency), using ModFit V3.0 software (Verity Software House, Topsham, ME, USA).

Statistical analysis

Data are presented as the mean ± standard deviation from at least three independent experiments. Statistical analysis of the data was performed by Student's t-test, one-way ANOVA using SPSS 17.0 software (SPSS, Inc., Chicago, IL, USA). P<0.05 (two-tailed) was considered to indicate a statistically significant difference.


Glycolysis is increased in activated fibroblasts from patients with oral carcinogenesis

To investigate the biological characteristic of fibroblasts isolated from oral premalignant and malignant lesions, IF staining for α-SMA was performed. A marked increase in α-SMA expression was observed in Dysplasia-fs and CAFs, compared with negative/low expression in NFs (Fig. 1A). These results indicated that fibroblasts were activated during oral carcinogenesis. Additionally, glucose and lactate assay kits were used to measure the levels of fibroblasts glycolysis. Glucose utilization and lactate production were increased significantly in CAFs compared with NFs (Fig. 1B).

Enhanced stromal glycolysis is cancer cell-dependent

To evaluate the association between stromal glycolysis and oral cancer cells, NFs and UM1 cells were co-cultured using a Transwell insert for 48 h, and then α-SMA staining was performed on the fibroblasts. As shown in Fig. 2A, fibroblasts were activated following cultivation with oral cancer cells and α-SMA expression of co-cultured fibroblasts was increased compared with fibroblasts without co-cultivation.

Activated fibroblasts were harvested after 48 h co-culture with CAL27, UM1 and SCC25 for subsequent analysis of glycolysis-associated gene expression. RT-qPCR and western blot results (Fig. 2B and C) showed that GLUT1, HK2, LDHA and MCT4 expression was increased in activated fibroblasts compared with fibroblasts cultured alone. Among these genes, GLUT1 was significantly upregulated with the highest fold change of mRNA level. Taken together, these data indicated that OSCC-activated fibroblasts displayed enhanced glycolysis, accompanied by an increase the expression of glycolysis associated genes. In our previous study, IL-1β was identified as a key node gene in OSCC progression, and elevated IL-1β expression was parallel with oral carcinogenesis (10). Thus, does IL-1β participate in stromal glycolysis induced by oral cancer cells?

IL-1β secretion from oral cancer cells is increased by activated fibroblasts

IL-1β mRNA expression was signifi-cantly increased in OSCC cell lines, compared with NOK cells (Fig. 3A). ELISA results demonstrated that UM1 and SCC25 cells secreted more IL-1β than NOK cells, and particularly that IL-1β secretion of UM1 was nearly twice that of NOK (Fig. 3B). However, CAL27 cells exhibited elevated IL-1β expression at the mRNA level only, with no significant alteration in IL-1β secretion detected by ELISA. Furthermore, when OSCC cells were co-cultured with fibroblasts (NFs), all the OSCC cell lines in our experiment expressed increasing IL-1β in a time-dependent manner, moreover, and UM1 cell was the most sensitive to the stimulation of fibroblasts (Fig. 4). Accordingly, the UM1 cell line was selected for subsequent IL-1β siRNA transfection experiments.

Enhanced stromal glycolysis in OSCC may be IL-1β-dependent

To determine the effect of IL-1β on tumor metabolism, IL-1β antagonists (IL-1Ra) was used to neutralize secreted IL-1β in the supernatant, and IL-1β siRNA was used to knock down endogenous IL-1β in OSCC cells, whereas exogenous recombinant human IL-1β was used to promote IL-1β-induced effects. OSCC cells and fibroblasts were treated with human recombination IL-1β (20 ng/ml) alone or both IL-1β (20 ng/ml) and IL-1Ra (20 mg/ml). CM were harvested at 6, 12, 24 and 48 h. No significant change in glucose consumption and lactate production was identified in OSCC cell lines following treatment. However, NFs and CAFs exhibited significantly increased glucose consumption after 24 h of IL-1β treatment, and lactate accumulation increased was after IL-1β treatment for 24 h in NFs and 48 h in CAFs. However, IL-1Ra significantly attenuated the IL-1β-induced effects on glucose consumption and lactate production in fibroblasts (Fig. 5A). Fibroblasts were harvested after IL-1β treatment for 48 h, and RT-qPCR assay was performed to investigate the expression of glycolysis-associated genes. As shown in Fig. 5B, GLUT1 and HK2 expression was significantly increased in the IL-1β treated group of NFs and CAFs. MCTs changed synergistically, with decreased expression of MCT1 and increased expression of MCT4, compared with untreated controls, respectively (Fig. 5B). However, when UM1 cells were transfected with si-IL-1β, GLUT1, LDHA and MCT4 expression significantly decreased, compared with the negative control siRNA group, (Fig. 5C). Collectively, these observations indicated that IL-1β stimulates glycolysis of activated oral fibroblasts.

Fibroblasts promote lactate uptake and proliferation of OSCC

The aforementioned findings demonstrated that oral cancer cells enhanced stromal glycolysis in the activated fibroblasts by secreting increased IL-1β, which resulted in MCT4 (a lactate excretion transporter) upregulation in fibroblasts. To further investigate the lactate destination and OSCC response to this, the lactate uptake transporter MCT1 expression and cell proliferation of OSCC cells in the co-culture system was examined. In UM1 and SCC25 cells, MCT1 protein expression increased in a time-dependent manner, and in CAL27 cells there was significant upregulation of MCT1 in the first passage of cultivation (Fig. 6A–C). UM1 cells were pre-stained with CFSE dye (which is equally distributed to two daughter cells during mitosis), and then co-cultured with NFs to detect the effect of stromal-epithelial lactate shuttle on OSCC cell proliferation. As shown in Fig. 6D, the proliferation index of UM1 cells in the co-culture group was significantly higher than that in UM1 cells cultured alone after 48 and 72 h (Fig. 6D). The above data suggest that lactate shuttle from activated oral fibroblasts to oral cancer cells promotes cancer cell proliferation.


Increasing evidence has highlighted the importance of reciprocal metabolic reprogramming and lactate shuttling in epithelial malignancies. However, the stromal-epithelial lactate shuttle and the underlying mechanisms during oral carcinogenesis still remain elusive. CAFs, also known as activated fibroblasts, are the biggest population of cancer stromal cells and differ from NFs in many respects, particularly epigenetics (12). For example, CAFs usually present with a caveolin-1 (cav-1) loss (13) and express active markers such as α-SMA, stromal cell derived factor-1 (14) and fibroblast activation protein (15). Gene expression analysis demonstrated that the activated fibroblasts, CAFs, secrete a large amount of proteins and enzymes that disrupt the extracellular matrix, recruit immunocytes, and promote angiogenesis and metastasis (16). The findings of the current study demonstrated that fibroblasts from different stages of OSCC progression, NFs, Dysplasia-fs and CAFs, displayed increased α-SMA expression, which suggested that the fibroblasts were activated during oral carcinogenesis. Additionally, these fibroblasts also exhibited increased glucose uptake and lactate accumulation in their supernatant, which indicated that glycolysis was enhanced fibroblasts from the TME. The increase in glycolysis in fibroblasts had been demonstrated in various solid human tumors (17). Pavlides et al (17), Bonuccelli et al (18) and Pavlides et al (19) reported that glycolytic enzymes were unregulated in CAFs with cav-1 loss, and they proposed that hydrogen peroxide secreted by cancer cells induced oxidative stress, mitophagy and aerobic glycolysis in CAFs.

It has been previously reported that cancer cells utilize fibroblast-produced intermediate products, such as lactate, ketone and glutamine, as nutrient substances (20). In human prostate cancer, tracing experiments explicitly demonstrated the lactate flows from fibroblasts to cancer cells in a common co-culture system. This metabolic symbiosis phenomenon was an important supplement to the Warburg effect, termed the 'reverse Warburg effect', which indicates that there must be a reciprocal metabolic influence between CAFs and cancer cells. In the current study, co-culture with OSCC cells significantly enhanced glycolytic gene expression in fibroblasts.

Our recent study identified IL-1β as a key node gene during oral carcinogenesis, both in epithelium and sub-mucosal fibroblasts. Notably, the IL-1β expression in epithelium increased gradually as oral malignancy progressed (10). Inversely, saliva exosome analysis of patients with OSCC revealed that secretory IL-1β significantly decreased following surgical treatment (21). OSCC cells were further confirmed as the source of intercellular IL-1β. In the current study, it was confirmed that IL-1β expression and secretion were upregulated in OSCC cell lines (UM1, SCC25 and CAL27). In the co-culture system, activated fibroblasts stimulated IL-1β expression in OSCC cells. Since the co-culture system imitated the epithelial-stromal interaction in vivo, it is deduced that activated fibroblasts participate in promoting IL-1β production in premalignant and malignant oral epithelium, and this substantial tumor-derived IL-1β may be a vital signal mediating epithelium-mesenchyme dialogue.

The results of the present study demonstrated that IL-1β expression in OSCC, activation of fibroblasts and aerobic glycolysis in fibroblasts were simultaneously enhanced during malignant progression of oral cancer cells. Does tumor-derived IL-1β enhance stromal glycolysis and induce lactate shuttle to the cancer cells? Further experiments demonstrated that exogenous IL-1β-treated NFs consumed more glucose and release more lactate into the supernatant. At the same time, the expression of glycolysis and lactate emission-associated genes, such as GLUT1, HK2, LDHA and MCT4, was increased in the IL-1β-treated NFs. Conversely, IL-Ra significantly abrogated the IL-1β-induced glycolysis. Knockdown using si-IL-1β in UM1 cells effectively blocked the regulatory effect of OSCC on stromal glycolysis. For OSCC cells in the co-culture system, the lactate uptake transporter, MCT1 was correspondingly overexpressed. These differentially expressed genes pointed to the reverse Warburg effect, because GLUT1 is the predominant facilitative glucose transporter in human cells, and overexpression of GLUT1 usually predicts increased glucose uptake (22,23). HK2 is a key rate-limiting enzyme in glycolysis, and LDHA catalyzes the conversion of pyruvate, a glycolysis mediator-production, into lactate (24,25). MCT1/4 are vital lactate transporters involved in acid-base balance, and promoting glucose metabolism in tumor tissues (26). MCT4, usually expressed in glycolytic cells, is especially enriched in cells of high oxygen consumption, while MCT1 is rather ubiquitous (5).

MCT4 overexpression in CAFs and MCT1 overexpression in transformed epithelium are regarded as independent indicators of poor outcomes in human carcinoma (27). The intercellular coordination of MCT1/4 expression in fibroblasts and cancer cells strongly indicate a unidirectional lactate shuttle, from stromal cells to the cancer cells (6,28,29). Thus, fibroblasts directly feed neighboring cancer cells via lactate. In this study, MCT4 in fibroblasts and MCT1 in OSCC cells were upregulated by the stromal-epithelial co-culture, suggesting that lactate may be transported to the oxidative cancer cells. Additionally, the proliferation of OSCC cells was accelerated following co-cultivation with the fibroblasts. All these findings support the regulatory function of IL-1β in the reverse Warburg effect and lactate reuse by cancer cells.

However, the underlying mechanism of IL-1β-modulated metabolic reprogramming remains ambiguous. Preliminarily results demonstrated that hypoxia inducible factor-1α (HIF-1α) may be partially responsible (data not shown), as IL-1β directly promoted HIF-1α expression in fibroblasts, which is a regulatory transcription factor of various metabolic genes (30). Other potential mechanism have also been reported, including that IL-1β induces accumulation of reactive oxygen species (12,31), and that IL-1β directly activates caspases in mitochondria (32), resulting in TCA cycle inhibition and promotes fibroblasts to utilize glucose through an inefficient method, anaerobic glycolysis.

In conclusion, the results of the present study identified a regulatory loop between fibroblasts and oral cancer cells by which cancer cells activate fibroblasts and fibroblasts promote IL-1β expression in OSCC. In turn, this tumor-derived IL-1β induces lactate emission from fibroblasts to feed cancer cells as 'fuel'. The findings provide novel insight into the role of IL-1β and lactate shuttle in oral cancer, and provide new therapeutic targets for future OSCC treatment.


This study was supported by grants of the National Natural Science Foundation of China (nos. 81272948, 81200787 and 81371148).



oral squamous cell carcinoma


cancer-associated fibroblasts


normal fibroblasts




α-smooth muscle actin


glucose transporter 1


hexokinase 2


lactic dehydrogenase


mono-carboxylate transporter 1


mono-carboxylate transporter 4


carboxyfluorescein succinimidyl ester



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February 2018
Volume 41 Issue 2

Print ISSN: 1107-3756
Online ISSN:1791-244X

2016 Impact Factor: 2.341
Ranked #21/128 Medicine Research and Experimental
(total number of cites)

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Wu, J., Hong, Y., Wu, T., Wang, J., Chen, X., Wang, Z. ... Xia, J. (2018). Stromal-epithelial lactate shuttle induced by tumor‑derived interleukin‑1β promotes cell proliferation in oral squamous cell carcinoma. International Journal of Molecular Medicine, 41, 687-696.
Wu, J., Hong, Y., Wu, T., Wang, J., Chen, X., Wang, Z., Cheng, B., Xia, J."Stromal-epithelial lactate shuttle induced by tumor‑derived interleukin‑1β promotes cell proliferation in oral squamous cell carcinoma". International Journal of Molecular Medicine 41.2 (2018): 687-696.
Wu, J., Hong, Y., Wu, T., Wang, J., Chen, X., Wang, Z., Cheng, B., Xia, J."Stromal-epithelial lactate shuttle induced by tumor‑derived interleukin‑1β promotes cell proliferation in oral squamous cell carcinoma". International Journal of Molecular Medicine 41, no. 2 (2018): 687-696.