Evidence map›Paper›PMID 38874683›Full record

ArticleBreast cancer research and treatment2024

Tamoxifen modulates nutrition deprivation-induced ER stress through AMPK-mediated ER-phagy in breast cancer cells.

Biswas Bidisha, Manickavasagan Sowmya, Suchita Shalini, Chandrasekaran Mythri, Anshu Gupta, Gangipangi Vijayakumar, Selvaraju Sudhagar

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Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

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3citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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3 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Biswas BidishaDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India.
Manickavasagan SowmyaDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India.
Suchita ShaliniDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India.
Chandrasekaran MythriDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India.
Anshu GuptaDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India.
Gangipangi VijayakumarDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India.
Selvaraju SudhagarDepartment of Biotechnology, National Institute of Pharmaceutical Education and Research - Guwahati, Changsari, India. sudhagar.s@niperguwahati.ac.in.

Funding

Department of Science and Technology, Ministry of Science and Technology, India CRG/2022/004934Indian Council of Medical Research 67/06/2022-DDI/BMS and 5/7/1745/CH/Adhoc/RBMCH-2021
6 · The paper itself

Abstract

purposeRapid proliferation and nutrition starvation in the tumor microenvironment pose significant challenges to cellular protein homeostasis. The accumulation of misfolded proteins in the endoplasmic reticulum lumen induces stress on cells and causes irreversible damage to cells if unresolved. Emerging reports emphasize the influence of the tumor microenvironment on therapeutic molecule efficacy and treatment outcomes. Hence, we aimed to understand the influence of tamoxifen on the cellular adaptation to endoplasmic reticulum stress during metabolic stress in breast cancer cells.

methodsNutrition deprivation induces endoplasmic reticulum stress (ER stress), and the unfolded protein response (UPR) in breast cancer cells was confirmed by a Thioflavin B assay and western blotting. Tamoxifen-indued ER-phagy was studied using an MCD assay, confocal microscopy, and western blotting.

resultsNutrition deprivation induces ER stress in breast cancer cells. Interestingly, tamoxifen modulates the nutrition deprivation-induced endoplasmic reticulum stress through enhancing the selective ER-phagy, a specialized autophagy. The tamoxifen-induced ER-phagy is mediated by AMPK activation. The pharmacological inhibition of AMPK blocks tamoxifen-induced ER-phagy and tamoxifen modulatory effect on ER stress during nutrition deprivation.

conclusionTamoxifen modulates ER stress by inducing ER-phagy through AMPK, thereby, may support breast cancer cell survival during nutrition deprivation conditions.

Indexed as

AMP-Activated Protein KinasesAutophagyBreast NeoplasmsEndoplasmic Reticulum StressTamoxifenUnfolded Protein ResponseAntineoplastic Agents, HormonalCell Line, TumorEndoplasmic ReticulumFemaleHumansMCF-7 CellsTumor MicroenvironmentAMP-Activated Protein KinasesAntineoplastic Agents, HormonalTamoxifenAMPKBreast cancerER-phagyER stressNutrition deprivationTamoxifen

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.