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Syntelin inhibits triple-negative breast cancer cell proliferation and metastasis
McKay Mullen1,2,† , Fengrui Yang1,2,† , Jun Cao1,* , Yang Cao3 , Xu Liu1,2 , Gee Young Lee2 , Tao Li1,4 , William Yao4 , Zhihong Yang1 , Jiahai Zhang1 , Kela Johnson2 , Felix Aikhionbare2 , Yong Chen3 , Xinjiao Gao1 , Dongmei Wang1 , Xia Ding4,* , Hadiyah-Nicole Green2,5,* , Xing Liu1,2,* , Xuebiao Yao1,2
1MOE Key Laboratory for Cellular Dynamics, Anhui Key Laboratory for Chemical Biology, CAS Center for Excellence in Molecular Cell Science, University of Science and Technology of China, Hefei 230027, China
2Keck Center for Oganoids Plasticity, Morehouse School of Medicine, Atlanta, GA 30310, USA
3Department of Hepatobiliary Surgery, Xijing Hospital, Xi’an 710032, China
4BUCM-USTC Collaborative Center for Parietal Cell Research, Beijing University of Chinese Medicine, Beijing 100029, China
5Ora Lee Smith Cancer Research Foundation, Atlanta, GA 30310, USA
These authors contributed equally to this work
*Correspondence to:Jun Cao , Email:caojun0811@ustc.edu.cn Xia Ding , Email:dingx@bucm.edu.cn Hadiyah-Nicole Green , Email:hgreen@msm.edu Xing Liu , Email:xing1017@ustc.edu.cn
J Mol Cell Biol, Volume 13, Issue 11, November 2021, 834-837,  https://doi.org/10.1093/jmcb/mjab054

Dear Editor,

The hallmarks of cancer comprise several distinct biological characteristics acquired during the multistep development of human tumors with the unique feature of genomic instability (Shen, 2011). These cancer characteristics include sustaining proliferative signaling, evading growth suppressors, resisting cell death, enabling replicative immortality, inducing angiogenesis, and activating invasion and metastasis (Chen et al., 2011; Song et al., 2018). Triple-negative breast cancer (TNBC), an aggressive disease with increased risks for visceral metastases, has a poor prognosis due to unavailable and viable therapeutic targets (Bianchini et al., 2016). A TNBC diagnosis indicates that cancer cells test negative for three key receptors: estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (Bianchini et al., 2016). The absence of these three receptors renders existing hormone and targeted therapies ineffective.