Targeting Autophagy and the Anticipatory Unfolded Protein Response Leads to Increased Breast Cancer Cell Death.

microPublication biology Pub Date : 2025-02-20 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001376
Jeffrey Brooks, Antonina Pizzo, Caela Fedraw, Florina Gojcaj, Myles Harris, Destiny Proffett, Ahed Anbari, Liselle Tungol, Mara R Livezey
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引用次数: 0

Abstract

Activation of the anticipatory unfolded protein response (aUPR) by the small molecule 3,3-bis(4-hydroxyphenyl)-7-methyl-1,3,dihydro-2H-indol-2-one (BHPI) leads to necrotic cell death in a variety of cancer cells containing Estrogen Receptor alpha (ERα). A key feature of BHPI's mechanism of action is depletion of cellular ATP. Other pathways such as autophagy can regulate cellular energy levels and ATP production. We present data that suggests targeting both the aUPR and autophagy leads to a significant increase in cell death in T47D and TYS breast cancer cells treated with BHPI. This combination presents itself as a possible therapeutic strategy against breast cancer.

靶向自噬和预期未折叠蛋白反应导致乳腺癌细胞死亡增加。
小分子3,3-二(4-羟基苯基)-7-甲基-1,3,二氢- 2h -吲哚-2- 1 (BHPI)激活预期未折叠蛋白反应(aUPR)可导致多种含有雌激素受体α (ERα)的癌细胞坏死细胞死亡。BHPI作用机制的一个关键特征是消耗细胞ATP。自噬等其他途径可以调节细胞能量水平和ATP的产生。我们提供的数据表明,同时靶向aUPR和自噬导致BHPI治疗的T47D和TYS乳腺癌细胞死亡的显著增加。这种组合本身就是一种可能的治疗乳腺癌的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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