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PRIMA-1不能恢复MDA-MB-231和MDA-MB-468三阴性乳腺癌细胞对维生素D的敏感性。

PRIMA-1 Does Not Restore Vitamin D Sensitivity to MDA-MB-231 and MDA-MB-468 Triple-Negative Breast Cancer Cells.

作者信息

Kotob Shadi N, Kelts Jessica L

机构信息

Department of Natural Sciences, University of Michigan-Flint, Flint, Michigan 48502, United States.

出版信息

ACS Omega. 2023 Aug 8;8(33):30500-30507. doi: 10.1021/acsomega.3c03719. eCollection 2023 Aug 22.

Abstract

Vitamin D is a steroid hormone that causes growth suppression in cultured cells. We had previously discovered that the triple-negative breast cancer cell lines MDA-MB-231 and MDA-MB-468 did not have growth suppression with vitamin D, while MCF-7 did. MCF-7 cells are not triple-negative and have wild-type p53. Both MDA-MB-231 and MDA-MB-468 have mutations in p53 and these mutations were a possible explanation for the lack of growth suppression with vitamin D. Our hypothesis was that reactivation of p53 in the triple-negative cell lines would cause them to become sensitive to vitamin D. We chose to use the small molecule PRIMA-1 to reactivate p53 as it has been previously shown to restore function to the p53 mutants present in MB-231 and MB-468. We then measured the ability of vitamin D and its analogues calcipotriol and EB1089 to suppress growth in the presence of PRIMA-1. Here, we show that while PRIMA-1 can kill the breast cancer cells investigated in this study, it does not restore their sensitivity to vitamin D or its analogues.

摘要

维生素D是一种类固醇激素,可抑制培养细胞的生长。我们之前发现,三阴性乳腺癌细胞系MDA-MB-231和MDA-MB-468对维生素D没有生长抑制作用,而MCF-7细胞系则有。MCF-7细胞不是三阴性的,且具有野生型p53。MDA-MB-231和MDA-MB-468的p53均有突变,这些突变可能是它们对维生素D缺乏生长抑制作用的原因。我们的假设是,在三阴性细胞系中重新激活p53会使它们对维生素D敏感。我们选择使用小分子PRIMA-1来重新激活p53,因为之前的研究表明它能恢复MB-231和MB-468中存在的p53突变体的功能。然后,我们测定了在PRIMA-1存在的情况下,维生素D及其类似物骨化三醇和EB1089抑制生长的能力。在此,我们表明,虽然PRIMA-1可以杀死本研究中所检测的乳腺癌细胞,但它并不能恢复这些细胞对维生素D或其类似物的敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd55/10448659/3edcaab5e936/ao3c03719_0002.jpg

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