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Survivin 抑制剂的发现 第 1 部分:筛选 Harbor Branch 纯化合物文库。

Discovery of Survivin Inhibitors Part 1: Screening the Harbor Branch Pure Compound Library.

机构信息

Harbor Branch Oceanographic Institute, Florida Atlantic University, 5600 US Highway 1, Fort Pierce, FL 34946, USA.

出版信息

Mar Drugs. 2021 Jan 30;19(2):73. doi: 10.3390/md19020073.

Abstract

Survivin is a 16.5 KDa protein whose functions include promoting cellular mitosis, angiogenesis, and senescence as well as inhibiting apoptosis. Higher survivin expression is found in cancer tissues than normal tissues, and this expression correlates with disease progression and aggressiveness. Survivin has been validated as a clinical target for cancer. Small molecules are important antagonists of survivin levels in cancer cells. A structurally diverse library of genetically encoded small molecules (natural products) derived from marine plants, invertebrates, and microbes was screened for their ability to reduce expression levels of survivin in the DLD-1 colon adenocarcinoma and the A549 nonsmall cell lung carcinoma cell lines. This led to the identification of this novel activity for the known compounds eryloside E, ilicicolin H, tanzawaic acid A, and -hydroxyphenopyrrozin. Both eryloside E and ilicicolin H showed the ability to reduce survivin expression in the low micromolar range against both cell lines.

摘要

生存素是一种 16.5 kDa 的蛋白质,其功能包括促进细胞有丝分裂、血管生成和衰老,以及抑制细胞凋亡。在癌症组织中发现的生存素表达高于正常组织,并且这种表达与疾病进展和侵袭性相关。生存素已被验证为癌症的临床治疗靶点。小分子是癌细胞中生存素水平的重要拮抗剂。从海洋植物、无脊椎动物和微生物中衍生的具有结构多样性的遗传编码小分子(天然产物)文库被筛选出其降低 DLD-1 结肠腺癌和 A549 非小细胞肺癌细胞系中生存素表达水平的能力。这导致已知化合物 eryloside E、ilicicolin H、tanzawaic acid A 和 -hydroxyphenopyrrozin 的这种新型活性的鉴定。eryloside E 和 ilicicolin H 均显示出在低微摩尔范围内针对两种细胞系降低生存素表达的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28c9/7911841/c11a0996ea5e/marinedrugs-19-00073-g001.jpg

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