The antidepressant imipramine inhibits breast cancer growth by targeting estrogen receptor signaling and DNA repair events. (1st August 2022)
- Record Type:
- Journal Article
- Title:
- The antidepressant imipramine inhibits breast cancer growth by targeting estrogen receptor signaling and DNA repair events. (1st August 2022)
- Main Title:
- The antidepressant imipramine inhibits breast cancer growth by targeting estrogen receptor signaling and DNA repair events
- Authors:
- Timilsina, Santosh
Rajamanickam, Subapriya
Rao, Arhan
Subbarayalu, Panneerdoss
Nirzhor, Saif
Abdelfattah, Nourhan
Viswanadhapalli, Suryavathi
Chen, Yidong
Jatoi, Ismail
Brenner, Andrew
Rao, Manjeet K.
Vadlamudi, Ratna
Kaklamani, Virginia - Abstract:
- Abstract: Aberrant activities of various cell cycle and DNA repair proteins promote cancer growth and progression and render them resistant to therapies. Here, we demonstrate that the anti-depressant imipramine blocks growth of triple-negative (TNBC) and estrogen receptor-positive (ER+) breast cancers by inducing cell cycle arrest and by blocking heightened homologous recombination (HR) and non-homologous end joining-mediated (NHEJ) DNA repair activities. Our results reveal that imipramine inhibits the expression of several cell cycle- and DNA repair-associated proteins including E2F1, CDK1, Cyclin D1, and RAD51. In addition, we show that imipramine inhibits the growth of ER + breast cancers by inhibiting the estrogen receptor- α (ER-α) signaling. Our studies in preclinical mouse models and ex vivo explants from breast cancer patients show that imipramine sensitizes TNBC to the PARP inhibitor olaparib and endocrine resistant ER + breast cancer to anti-estrogens. Our studies suggest that repurposing imipramine could enhance routine care for breast cancer patients. Based on these results, we designed an ongoing clinical trial, where we are testing the efficacy of imipramine for treating patients with triple-negative and estrogen receptor-positive breast cancer. Since aberrant DNA repair activity is used by many cancers to survive and become resistant to therapy, imipramine could be used alone and/or with currently used drugs for treating many aggressive cancers. Highlights:Abstract: Aberrant activities of various cell cycle and DNA repair proteins promote cancer growth and progression and render them resistant to therapies. Here, we demonstrate that the anti-depressant imipramine blocks growth of triple-negative (TNBC) and estrogen receptor-positive (ER+) breast cancers by inducing cell cycle arrest and by blocking heightened homologous recombination (HR) and non-homologous end joining-mediated (NHEJ) DNA repair activities. Our results reveal that imipramine inhibits the expression of several cell cycle- and DNA repair-associated proteins including E2F1, CDK1, Cyclin D1, and RAD51. In addition, we show that imipramine inhibits the growth of ER + breast cancers by inhibiting the estrogen receptor- α (ER-α) signaling. Our studies in preclinical mouse models and ex vivo explants from breast cancer patients show that imipramine sensitizes TNBC to the PARP inhibitor olaparib and endocrine resistant ER + breast cancer to anti-estrogens. Our studies suggest that repurposing imipramine could enhance routine care for breast cancer patients. Based on these results, we designed an ongoing clinical trial, where we are testing the efficacy of imipramine for treating patients with triple-negative and estrogen receptor-positive breast cancer. Since aberrant DNA repair activity is used by many cancers to survive and become resistant to therapy, imipramine could be used alone and/or with currently used drugs for treating many aggressive cancers. Highlights: How about this? I just tried to break it up to be shorter points. . Anti-depressant imipramine blocks the growth and progression of breast cancers. Imipramine induces cell cycle arrest and blocks heightened DNA repair activities in breast cancer cells. Imipramine blocked the ER-α signaling and improved the efficacy of anti-estrogen in ER + breast cancers. Imipramine improved the efficacy of PARP inhibitor in TNBC. … (more)
- Is Part Of:
- Cancer letters. Volume 540(2022)
- Journal:
- Cancer letters
- Issue:
- Volume 540(2022)
- Issue Display:
- Volume 540, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 540
- Issue:
- 2022
- Issue Sort Value:
- 2022-0540-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-08-01
- Subjects:
- Imipramine -- Drug repurposing -- Breast cancer -- DNA damage -- DNA repair -- Estrogen receptor
Cancer -- Periodicals
Neoplasms -- Periodicals
Cancer -- Périodiques
Electronic journals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03043835/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.canlet.2022.215717 ↗
- Languages:
- English
- ISSNs:
- 0304-3835
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.485000
British Library DSC - BLDSS-3PM
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- 21566.xml