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一种靶向ROR1的小分子用于治疗三阴性乳腺癌的鉴定与验证

Identification and validation of a small molecule targeting ROR1 for the treatment of triple negative breast cancer.

作者信息

Gupta Shradheya R R, Ta Tram M, Khan Maryam, Singh Archana, Singh Indrakant K, Peethambaran Bela

机构信息

Molecular Biology Research Laboratory, Department of Zoology, Deshbandhu College, University of Delhi, New Delhi, India.

Department of Biology, Saint Joseph's University, Philadelphia, PA, United States.

出版信息

Front Cell Dev Biol. 2023 Sep 13;11:1243763. doi: 10.3389/fcell.2023.1243763. eCollection 2023.

Abstract

Breast cancer is the most common cancer in women, with roughly 10-15% of new cases classified as triple-negative breast cancer (TNBC). Traditional chemotherapies are often toxic to normal cells. Therefore, it is important to discover new anticancer compounds that target TNBC while causing minimal damage to normal cells. Receptor tyrosine kinase-like Orphan Receptor 1 (ROR1) is an oncofetal protein overexpressed in numerous human malignancies, including TNBC. This study investigated potential small molecules targeting ROR1. Using AutoDock Vina and Glide, we screened 70,000 chemicals for our investigation. We obtained 10 representative compounds via consensus voting, deleting structural alerts, and clustering. After manual assessment, compounds 2 and 4 were chosen for MD simulation and cell viability experiment. Compound 4 showed promising results in the viability assay, which led us to move further with the apoptosis assay and immunoblotting. Compound 4 (CID1261330) had docking scores of -6.635 and -10.8. It fits into the pocket and shows interactions with GLU64, ASP174, and PHE93. Its RMSD fluctuates around 0.20 nm and forms two stable H-bonds indicating compound 4 stability. It inhibits cell proliferation in MDA-MB-231, HCC1937, and HCC1395 cell lines, with IC values of approximately 2 μM to 10 μM, respectively. Compound 4 did not kill non-malignant epithelial breast cells MCF-10A (IC > 27 μM). These results were confirmed by the significant number of apoptotic cells in MDA-MB-231 cells (47.6%) but not in MCF-10A cells (7.3%). Immunoblot analysis provided additional support in the same direction. These findings collectively suggest that compound 4 has the potential to effectively eliminate TNBC cells while causing minimal harm to normal breast cells. The promising outcomes of this study lay the groundwork for further testing of compound 4 in other malignancies characterized by ROR1 upregulation, serving as a proof-of-concept for its broader applicability.

摘要

乳腺癌是女性中最常见的癌症,约10%-15%的新发病例被归类为三阴性乳腺癌(TNBC)。传统化疗通常对正常细胞有毒性。因此,发现能够靶向TNBC同时对正常细胞造成最小损害的新型抗癌化合物非常重要。受体酪氨酸激酶样孤儿受体1(ROR1)是一种癌胚蛋白,在包括TNBC在内的多种人类恶性肿瘤中过表达。本研究调查了靶向ROR1的潜在小分子。使用AutoDock Vina和Glide,我们筛选了70000种化学物质用于研究。通过共识投票、删除结构警示和聚类,我们获得了10种代表性化合物。经过人工评估后,选择化合物2和4进行分子动力学模拟和细胞活力实验。化合物4在活力测定中显示出有前景的结果,这促使我们进一步进行凋亡测定和免疫印迹分析。化合物4(CID1261330)的对接分数分别为-6.635和-10.8。它适合进入口袋,并与GLU64、ASP174和PHE93显示相互作用。其均方根偏差(RMSD)在0.20nm左右波动,并形成两个稳定的氢键,表明化合物4的稳定性。它抑制MDA-MB-231、HCC1937和HCC1395细胞系中的细胞增殖,IC值分别约为2μM至10μM。化合物4不会杀死非恶性上皮性乳腺细胞MCF-10A(IC>27μM)。MDA-MB-231细胞中大量凋亡细胞(47.6%)而MCF-10A细胞中凋亡细胞较少(7.3%)证实了这些结果。免疫印迹分析在同一方向上提供了额外支持。这些发现共同表明,化合物4有潜力有效消除TNBC细胞,同时对正常乳腺细胞造成最小伤害。本研究的有前景结果为化合物4在其他以ROR1上调为特征的恶性肿瘤中的进一步测试奠定了基础,为其更广泛的适用性提供了概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4478/10534069/c55ec38f2d97/fcell-11-1243763-g001.jpg

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