| Literature DB >> 27123089 |
Hongyong Jin1, Sujie Gao2, Huiling Guo1, Shengnan Ren1, Fujian Ji1, Zhuo Liu1, Xuebo Chen1.
Abstract
Radiotherapy (RT) is commonly used to treat multi-tumors to attenuate the risk of recurrence. Despite impressive initial clinical responses, a large proportion of patients experience resistance to RT. Therefore, identification of functionally relevant biomarkers would be beneficial for radioresistant patients. Adenosine monophosphate-activated kinase (AMPK) is recognized as a mediator of tumor suppressor gene function. In the present study, radio-sensitive and -resistant colon cancer patient samples were compared and the AMPK pathway was observed to be highly activated in radioresistant patients. In addition, the protein and mRNA levels of AMPK were upregulated in radioresistant colon cancer cells in comparison to radiosensitive colon cancer cells. The present study provides evidence that activation of AMPK by metformin contributes to radioresistance. Inhibition of AMPK by either small interfering RNA or Compound C, which is a specific inhibitor of AMPK, re-sensitized radiation resistant cells. The data presented indicates a synergistic effect on radiation resistant cancer cells by the combination of Compound C and radiation. In summary, the present study proposes that inhibition of the AMPK pathway is a potential strategy for reversing radiation resistance and may contribute to the development of therapeutic anticancer drugs.Entities:
Keywords: AMPK; colorectal cancer; compound C; metformin; radioresistance
Year: 2016 PMID: 27123089 PMCID: PMC4841055 DOI: 10.3892/ol.2016.4339
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967