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- Title
Inhibition of mTORC1 through ATF4-induced REDD1 and Sestrin2 expression by Metformin.
- Authors
Jang, Se-Kyeong; Hong, Sung-Eun; Lee, Da-Hee; Kim, Ji-Young; Kim, Ji Yea; Ye, Sang-Kyu; Hong, Jungil; Park, In-Chul; Jin, Hyeon-Ok
- Abstract
<bold>Background: </bold>Although the major anticancer effect of metformin involves AMPK-dependent or AMPK-independent mTORC1 inhibition, the mechanisms of action are still not fully understood.<bold>Methods: </bold>To investigate the molecular mechanisms underlying the effect of metformin on the mTORC1 inhibition, MTT assay, RT-PCR, and western blot analysis were performed.<bold>Results: </bold>Metformin induced the expression of ATF4, REDD1, and Sestrin2 concomitant with its inhibition of mTORC1 activity. Treatment with REDD1 or Sestrin2 siRNA reversed the mTORC1 inhibition induced by metformin, indicating that REDD1 and Sestrin2 are important for the inhibition of mTORC1 triggered by metformin treatment. Moreover, REDD1- and Sestrin2-mediated mTORC1 inhibition in response to metformin was independent of AMPK activation. Additionally, lapatinib enhances cell sensitivity to metformin, and knockdown of REDD1 and Sestrin2 decreased cell sensitivity to metformin and lapatinib.<bold>Conclusions: </bold>ATF4-induced REDD1 and Sestrin2 expression in response to metformin plays an important role in mTORC1 inhibition independent of AMPK activation, and this signalling pathway could have therapeutic value.
- Subjects
METFORMIN; WESTERN immunoblotting; RESPONSE inhibition
- Publication
BMC Cancer, 2021, Vol 21, Issue 1, p1
- ISSN
1471-2407
- Publication type
journal article
- DOI
10.1186/s12885-021-08346-x