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锚蛋白重复结构域1通过激活核因子-κB-黑色素瘤抗原基因A6通路促进乳腺癌转移。

ANKRD1 Promotes Breast Cancer Metastasis by Activating NF-B-MAGE-A6 Pathway.

作者信息

Diskul-Na-Ayudthaya Penchatr, Bae Seon Joo, Bae Yun-Ui, Van Ngu Trinh, Kim Wootae, Ryu Seongho

机构信息

Soonchunhyang Institute of Medi-bio Science (SIMS), Department of Integrated Biomedical Sciences, Soonchunhyang University, Asan-si 31151, Republic of Korea.

Laboratory of Biochemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.

出版信息

Cancers (Basel). 2024 Sep 27;16(19):3306. doi: 10.3390/cancers16193306.

Abstract

Early detection and surgical excision of tumors have helped improve the survival rate of patients with breast cancer. However, patients with metastatic cancer typically have a poor prognosis. In this study, we propose that ANKRD1 promotes metastasis of breast cancer. ANKRD1 was found to be highly expressed in the MDA-MB-231 and MDA-LM-2 highly metastatic breast cancer cell lines compared to the non-metastatic breast cancer cell lines (MCF-7, ZR-75-30, T47D) and normal breast cancer cells (MCF-10A). Furthermore, high-grade tumors showed increased levels of ANKRD1 compared to low-grade tumors. Both in vitro and in vivo functional studies demonstrated the essential role of ANKRD1 in cancer cell migration and invasion. The previous studies have suggested a significant role of NF-κB and MAGE-A6 in breast cancer metastasis, but the upstream regulators of this axis are not well characterized. Our study suggests that ANKRD1 promotes metastasis of breast cancer by activating NF-κB as well as MAGE-A6 signaling. Our findings show that ANKRD1 is a potential therapeutic target and a diagnostic marker for breast cancer metastasis.

摘要

肿瘤的早期检测和手术切除有助于提高乳腺癌患者的生存率。然而,转移性癌症患者的预后通常较差。在本研究中,我们提出ANKRD1促进乳腺癌转移。与非转移性乳腺癌细胞系(MCF-7、ZR-75-30、T47D)和正常乳腺细胞(MCF-10A)相比,发现ANKRD1在MDA-MB-231和MDA-LM-2高转移性乳腺癌细胞系中高表达。此外,与低级别肿瘤相比,高级别肿瘤中ANKRD1水平升高。体外和体内功能研究均证明ANKRD1在癌细胞迁移和侵袭中起重要作用。先前的研究表明NF-κB和MAGE-A6在乳腺癌转移中起重要作用,但该轴的上游调节因子尚未得到很好的表征。我们的研究表明,ANKRD1通过激活NF-κB以及MAGE-A6信号通路促进乳腺癌转移。我们的研究结果表明,ANKRD1是乳腺癌转移的潜在治疗靶点和诊断标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f57/11476229/4f7f23001292/cancers-16-03306-g001.jpg

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