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合成姜黄素类似物HO-3867可挽救卵巢癌细胞中PLAC1表达的抑制。

The Synthetic Curcumin Analog HO-3867 Rescues Suppression of PLAC1 Expression in Ovarian Cancer Cells.

作者信息

Devor Eric J, Schickling Brandon M, Lapierre Jace R, Bender David P, Gonzalez-Bosquet Jesus, Leslie Kimberly K

机构信息

Department of Obstetrics and Gynecology, University of Iowa, Carver College of Medicine, Iowa City, IA 52242, USA.

Holden Comprehensive Cancer Center, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA.

出版信息

Pharmaceuticals (Basel). 2021 Sep 21;14(9):942. doi: 10.3390/ph14090942.

Abstract

Elevated expression of placenta-specific protein 1 (PLAC1) is associated with the increased proliferation and invasiveness of a variety of human cancers, including ovarian cancer. Recent studies have shown that the tumor suppressor p53 directly suppresses PLAC1 transcription. However, mutations in p53 lead to the loss of PLAC1 transcriptional suppression. Small molecules that structurally convert mutant p53 proteins to wild-type conformations are emerging. Our objective was to determine whether the restoration of the wild-type function of mutated p53 could rescue PLAC1 transcriptional suppression in tumors harboring certain mutations. Ovarian cancer cells OVCAR3 and ES-2, both harboring missense mutations, were treated with the p53 reactivator HO-3867. Treatment with HO-3867 successfully rescued PLAC1 transcriptional suppression. In addition, cell proliferation was inhibited and cell death through apoptosis was increased in both cell lines. We conclude that the use of HO-3867 as an adjuvant to conventional therapeutics in ovarian cancers harboring TP53 missense mutations could improve patient outcomes. Validation of this conclusion must, however, come from an appropriately designed clinical trial.

摘要

胎盘特异性蛋白1(PLAC1)的高表达与包括卵巢癌在内的多种人类癌症的增殖和侵袭性增加有关。最近的研究表明,肿瘤抑制因子p53直接抑制PLAC1转录。然而,p53突变会导致PLAC1转录抑制功能丧失。能够将突变型p53蛋白转化为野生型构象的小分子正在出现。我们的目的是确定突变型p53野生型功能的恢复是否能挽救携带特定突变的肿瘤中PLAC1的转录抑制。对携带错义突变的卵巢癌细胞OVCAR3和ES-2用p53激活剂HO-3867进行处理。HO-3867处理成功挽救了PLAC1的转录抑制。此外,两种细胞系中的细胞增殖均受到抑制,且通过凋亡导致的细胞死亡增加。我们得出结论,在携带TP53错义突变的卵巢癌中,使用HO-3867作为传统疗法的辅助药物可能会改善患者预后。然而,这一结论必须通过适当设计的临床试验来验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4517/8465575/6f22b3df7b86/pharmaceuticals-14-00942-g001.jpg

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