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PI3K/Akt/mTOR activation by suppression of ELK3 mediates chemosensitivity of MDA-MB-231 cells to doxorubicin by inhibiting autophagy
- Park, Ji-Hoon;
- Kim, Keun Pil;
- Ko, Jeong-Jae;
- Park, Kyung-Soon
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46초록
Drug resistance in breast cancer remains a major obstacle of clinical therapy. We found that suppression of ELK3 in the triple negative breast cancer cell line MDA-MB-231 impaired autophagy and led to a hypersensitive response to doxorubicin treatment. In ELK3-knockdown MDA-MB-231 cells (ELK3 KD), autophagy was not activated under starvation conditions, which is a major stimulus of autophagy activation. We revealed that activation of the PI3K/Akt pathway was the main cause of impaired autophagy in ELK3 KD. Our results suggest that targeting ELK3 may be a potential approach to overcome doxorubicin resistance in breast cancer therapeutics. (C) 2016 Published by Elsevier Inc.
키워드
Autophagy; Doxorubicin; ELK3; MDA-MB-231 cell line; PI3K/Akt; ADVANCED SOLID TUMORS; BREAST-CANCER CELLS; PHASE-I TRIAL; HYDROXYCHLOROQUINE; APOPTOSIS; PATHWAY; KINASE; NET; TRANSCRIPTION; TEMOZOLOMIDE
- 제목
- PI3K/Akt/mTOR activation by suppression of ELK3 mediates chemosensitivity of MDA-MB-231 cells to doxorubicin by inhibiting autophagy
- 저자
- Park, Ji-Hoon; Kim, Keun Pil; Ko, Jeong-Jae; Park, Kyung-Soon
- 발행일
- 2016-08
- 유형
- Article
- 권
- 477
- 호
- 2
- 페이지
- 277 ~ 282
- 언어
- ENG
- 출판사
- ACADEMIC PRESS INC ELSEVIER SCIENCE
- 발행국가
- 미국
- 분량
- 6 페이지
- ISSN
- E 1090-2104
P 0006-291X