| Literature DB >> 29477380 |
Ying Shi1, Na Liu1, Weiwei Lai1, Bin Yan1, Ling Chen1, Shouping Liu1, Shuang Liu2, Xiang Wang3, Desheng Xiao4, Xiaoli Liu1, Chao Mao1, Yiqun Jiang1, Jiantao Jia5, Yating Liu1, Rui Yang1, Ya Cao1, Yongguang Tao6.
Abstract
Radiation therapy has become an important tool in the treatment of cancer patients, but most patients relapse within 5 years. Relapse is due to the presence of cancer stem cells (CSCs), but the molecular mechanism of radioresistance in CSCs remains largely elusive. Here, we found that irradiation-resistant (IR) cells exhibited increased stem cell-like properties together with elevated anchorage-independent growth and metastasis ability. EGFR not only leads to increased acquisition of endometrial cancer stem cell markers in radioresistant sublines but is critical for the cancer stem-cell phenotype and tumorigenicity. Moreover, PKM2 functions as an interacting partner of EGFR, which induces the EMT phenotype and stem cell-like properties in IR cells. Finally, we found that the regulatory function of the EGFR-PKM2 axis is dependent on nuclear EGFR. In sum, our study indicated that EGFR and PKM2 directly interact and bind with each other to regulate the transcription of stemness-related genes and promote the stem-like phenotype, thus promoting invasion and metastasis.Entities:
Keywords: EGFR; Metastasis; PKM2; Radioresistance; Stem-like
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Year: 2018 PMID: 29477380 DOI: 10.1016/j.canlet.2018.02.028
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679