Autophagy promotes metastasis and glycolysis by upregulating MCT1 expression and Wnt/β-catenin signaling pathway activation in hepatocellular carcinoma cells
Open accessAbstract
Autophagy is a dynamic physiological process that can generate energy and nutrients for cell survival during stress. Autophagy can regulate the migration and invasive ability in cancer cells. However, the connection between autophagy and metabolism is unclear. Monocarboxylate transporter 1 (MCT1) plays an important role in lactic acid transport and H + clearance in cancer cells, and Wnt/β-catenin signaling can increase cancer cell glycolysis. We investigated whether autophagy promotes glycolysis in hepatocellular carcinoma (HCC) cells by activating the Wnt/β-catenin signaling pathway, accompanied by MCT1 upregulation. Autophagic activity was evaluated using western blotting, immunoblotting, and transmission electron microscopy. The underlying mechanisms of autophagy activation on HCC cell glycolysis were studied via western blotting, and Transwell, lactate, and glucose assays. MCT1 expression was detected using quantitative reverse transcription–PCR (real-time PCR), western blotting, and immunostaining of HCC tissues and the paired adjacent tissues. Autophagy promoted HCC cell glycolysis accompanied by MCT1 upregulation. Wnt/β-catenin signaling pathway activation mediated the effect of autophagy on HCC cell glycolysis. β-Catenin downregulation inhibited the autophagy-induced glycolysis in HCC cells, and reduced MCT1 expression in the HCC cells. MCT1 was highly expressed in HCC tissues, and high MCT1 expression correlated positively with the expression of microtubule-associated protein light chain 3 (LC3). Activation of autophagy can promote metastasis and glycolysis in HCC cells, and autophagy induces MCT1 expression by activating Wnt/β-catenin signaling. Our study describes the connection between autophagy and glucose metabolism in HCC cells and may provide a potential therapeutic target for HCC treatment.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Autophagy promotes glycolysis in HCC cells by upregulating MCT1.
“Furthermore, autophagy has been shown to promote glycolysis in hepatocellular carcinoma (HCC) cells by upregulating monocarboxylate transporter 1 (MCT1), which plays an important role in the transport of lactic acid170.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [170]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 retracted
TUSC3 induces autophagy in human non-small cell lung cancer cells through Wnt/β-catenin signaling
Peng, Y., Cao, J., Yao, X., Wang, J., Zhong, M., Gan, P., & Li, J. (2017) · Oncotarget · doi:10.18632/oncotarget.17674 · Cited by 30 · see citing works
RetractedLevy, J. M. M., Towers, C. G., & Thorburn, A. (2017) · Nature Reviews Cancer · doi:10.1038/nrc.2017.53 · Cited by 2,526 · see citing works
The role for autophagy in cancer
White, E. (2015) · Journal of Clinical Investigation · doi:10.1172/jci73941 · Cited by 1,332 · see citing works
Jiang, P., & Mizushima, N. (2013) · Cell Research · doi:10.1038/cr.2013.161 · Cited by 767 · see citing works
Autophagy facilitates glycolysis during Ras-mediated oncogenic transformation
Lock, R., Roy, S., Kenific, C. M., Su, J. S., Salas, E., Ronen, S. M., & Debnath, J. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-06-0500 · Cited by 467 · see citing works
Wnt signaling directs a metabolic program of glycolysis and angiogenesis in colon cancer
Pate, K. T., Stringari, C., Sprowl‐Tanio, S., Wang, K., TeSlaa, T., Hoverter, N. P., McQuade, M. M., Garner, C., Digman, M. A., Teitell, M. A., et al. (2014) · The EMBO Journal · doi:10.15252/embj.201488598 · Cited by 459 · see citing works
Heterogeneity of liver cancer and personalized therapy
Li, L., & Wang, H. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.07.018 · Cited by 340 · see citing works
Autophagy-Dependent Production of Secreted Factors Facilitates Oncogenic RAS-Driven Invasion
Lock, R., Kenific, C. M., Leidal, A. M., Salas, E., & Debnath, J. (2014) · Cancer Discovery · doi:10.1158/2159-8290.cd-13-0841 · Cited by 280 · see citing works
Galavotti, S., Bartesaghi, S., Faccenda, D., Shaked-Rabi, M., Sanzone, S., McEvoy, A. W., Dinsdale, D. D., Condorelli, F., Brandner, S., Campanella, M., et al. (2012) · Oncogene · doi:10.1038/onc.2012.111 · Cited by 266 · see citing works
Wickström, M., Dyberg, C. H., Milosevic, J., Einvik, C., Calero, R., Sveinbjørnsson, B., Sandén, E., Darabi, A., Siesjö, P., Kool, M., et al. (2015) · Nature Communications · doi:10.1038/ncomms9904 · Cited by 229 · see citing works
MCT1 Modulates Cancer Cell Pyruvate Export and Growth of Tumors that Co-express MCT1 and MCT4
Hong, C. S., Graham, N. A., Gu, W., Camacho, C. E., Mah, V. H., Maresh, E. L., Alavi, M., Bagryanova, L., Krotee, P., Gardner, B. K., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.01.057 · Cited by 223 · see citing works
Beyoğlu, D., Imbeaud, S., Maurhofer, O., Bioulac‐Sage, P., Zucman‐Rossi, J., Dufour, J., & Idle, J. R. (2013) · Hepatology · doi:10.1002/hep.26350 · Cited by 214 · see citing works
Emerging Signaling Pathways in Hepatocellular Carcinoma
Moeini, A., Cornellà, H., & Villanueva, A. (2012) · Liver Cancer · doi:10.1159/000342405 · Cited by 195 · see citing works
Current and future treatments for hepatocellular carcinoma
Schlachterman, A. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i28.8478 · Cited by 171 · see citing works
The role of autophagy in hepatocellular carcinoma: friend or foe
Liu, L., Liao, J., He, X., & Li, P. (2017) · Oncotarget · doi:10.18632/oncotarget.17202 · Cited by 155 · see citing works
Yang, L., Zhang, X., Li, H., & Liu, J. (2016) · Molecular BioSystems · doi:10.1039/c6mb00114a · Cited by 152 · see citing works
Self-citationAutophagy in lung disease pathogenesis and therapeutics
Ryter, S. W., & Choi, A. M. K. (2015) · Redox Biology · doi:10.1016/j.redox.2014.12.010 · Cited by 137 · see citing works
Hashimoto, D., Bläuer, M., Hirota, M., Ikonen, N. H., Sand, J. A., & Laukkarinen, J. (2014) · European Journal of Cancer · doi:10.1016/j.ejca.2014.01.011 · Cited by 116 · see citing works
The Autophagy-Related Marker LC3 Can Predict Prognosis in Human Hepatocellular Carcinoma
Lee, Y. J., Ha, Y. J., Kang, Y. N., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081540 · Cited by 90 · see citing works
Vallée, A., Lecarpentier, Y., Guillevin, R., & Vallée, J.-N. (2017) · Journal of Molecular Neuroscience · doi:10.1007/s12031-017-0947-4 · Cited by 80 · see citing works
β-Catenin Knockdown Affects Mitochondrial Biogenesis and Lipid Metabolism in Breast Cancer Cells
Vergara, D., Stanca, E., Guerra, F., Priore, P., Gaballo, A., Franck, J., Simeone, P., Trerotola, M., Domenico, S. D., Fournier, I., et al. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00544 · Cited by 75 · see citing works
Dovmark, T. H., Saccomano, M., Hulikova, A., Alves, F., & Swietach, P. (2017) · Oncogene · doi:10.1038/onc.2017.71 · Cited by 74 · see citing works
Role of hypoxia and autophagy in MDA‐MB‐231 invasiveness
Indelicato, M., Pucci, B., Schito, L., Reali, V., Aventaggiato, M., Mazzarino, M. C., Stivala, F., Fini, M., Russo, M. A., & Tafani, M. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.22041 · Cited by 67 · see citing works
Autophagy enhances hepatocellular carcinoma progression by activation of mitochondrial β-oxidation
Toshima, T., Shirabe, K., Matsumoto, Y., Yoshiya, S., Ikegami, T., Yoshizumi, T., Soejima, Y., Ikeda, T., & Maehara, Y. (2013) · Journal of Gastroenterology · doi:10.1007/s00535-013-0835-9 · Cited by 64 · see citing works
Zhang, J., Lai, W., Li, Q., et al. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.07.041 · Cited by 59 · see citing works
Role of insulin receptor substrates in the progression of hepatocellular carcinoma
Sakurai, Y., Kubota, N., Takamoto, I., Obata, A., Iwamoto, M., Hayashi, T., Aihara, M., Kubota, T., Nishihara, H., & Kadowaki, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-03299-3 · Cited by 51 · see citing works
Autophagy and Heart Disease: Implications for Cardiac Ischemia- Reperfusion Damage
Ghavami, S., Gupta, S., Ambrose, E., et al. (2014) · Current Molecular Medicine · doi:10.2174/1566524014666140603101520 · Cited by 50 · see citing works
Pedersen, S. F., Kramhøft, B., Jørgensen, N. K., & Hoffmann, E. K. (1996) · The Journal of Membrane Biology · doi:10.1007/s002329900015 · Cited by 49 · see citing works
Mathematical modeling links Wnt signaling to emergent patterns of metabolism in colon cancer
Lee, M. M., Chen, G. T., Puttock, E. J., Wang, K., Edwards, R. A., Waterman, M. L., & Lowengrub, J. S. (2017) · Molecular Systems Biology · doi:10.15252/msb.20167386 · Cited by 39 · see citing works
Development and novel therapeutics in hepatocellular carcinoma: a review
Ingle, P. V., Samsudin, S. Z. B., Qi, C. P., et al. (2016) · Therapeutics and Clinical Risk Management · doi:10.2147/tcrm.s92377 · Cited by 36 · see citing works
Tumor bioenergetics: An emerging avenue for cancer metabolism targeted therapy
Kee, H. J., & Cheong, J. (2014) · BMB Reports · doi:10.5483/bmbrep.2014.47.3.273 · Cited by 32 · see citing works
Wu, W., Kim, H., Zhang, C., Meng, X.-L., & Wu, Z. (2014) · Medical Oncology · doi:10.1007/s12032-014-0108-3 · Cited by 29 · see citing works
Oncogenic MCT-1 activation promotes YY1-EGFR-MnSOD signaling and tumor progression
Tseng, H.-Y., Chen, Y., Jen, J., Shen, P.-C., Chen, L., Lin, T.-D., Wang, Y.-C., & Hsu, H. L. (2017) · Oncogenesis · doi:10.1038/oncsis.2017.13 · Cited by 29 · see citing works
Yen, C., Lai, C.-C., Shia, T.-H., et al. (2017) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2017.07.019 · Cited by 28 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Glutamine reliance in cell metabolism
Yoo, H. C., Yu, Y. C., Sung, Y., & Han, J. M. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-00504-8 · Cited by 1,021 · see citing works
The Role of the Extracellular Matrix in Cancer Stemness
Nallanthighal, S., Heiserman, J. P., & Cheon, D.-J. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00086 · Cited by 344 · see citing works
- Authors
- Fan, Q., Yang, L., Zhang, X., Ma, Y., Li, Y., Dong, L., Zong, Z., Hua, X., Su, D., Li, H., & Liu, J.
- Affiliations
- Fourth Affiliated Hospital of China Medical University (CN)
- Dalian Medical University (CN)
- Liaoning Cancer Hospital & Institute (CN)
- Second Affiliated Hospital of Nanjing Medical University (CN)
- Corresponding author
- Li, Hangyu
- Liu, Jingang
- ORCID
- Venue
- Journal of Experimental & Clinical Cancer Research
- Published
- 2018-01-19
- Volume
- 37
- Issue
- 1
- Pages
- 9-9
- ISSN
- 0392-9078 (ISSN-L)
- 1756-9966
- PMC
- PMC5775607
- OpenAlex
- W2784901213
- Cited by
- 216
- References
- 34
- Citations by year
- 2026: 16 · 2025: 21 · 2024: 50 · 2023: 30 · 2022: 26 · 2021: 34 · 2020: 21 · 2019: 10 · 2018: 8
- FWCI
- 14.82
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Journal of Experimental & Clinical Cancer Research (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (81472303, 81572425)
- Topics
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Keywords
- autophagy, hepatocellular carcinoma, MCT1, Wnt/β-catenin signaling, glycolysis, cancer metabolism, metastasis, LC3, glucose metabolism
- MeSH terms
- Monocarboxylate Transport Protein 1, Autophagy, Glucose, Glycolysis, Carcinoma, Hepatocellular, Humans, Liver Neoplasms, Models, Biological, Gene Expression, Gene Expression Regulation, Neoplastic, Genes, Reporter, Monocarboxylic Acid Transporters, Symporters, Cell Line, Tumor, Cell Proliferation, Wnt Signaling Pathway
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review