A new small cell lung cancer biomarker identified by Cell-SELEX generated aptamers

被引:19
|
作者
Zhou, Wei [1 ,2 ]
Zhao, Libo [1 ,6 ]
Yuan, Hongyu [3 ,4 ]
Xu, Li [1 ]
Tan, Weihong [5 ]
Song, Yongmei [3 ,4 ]
Fang, Xiaohong [1 ,2 ]
机构
[1] Chinese Acad Sci, Beijing Natl Res Ctr Mol Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Chinese Acad Med Sci, Natl Canc Ctr, Canc Hosp, Beijing 100021, Peoples R China
[4] Peking Union Med Coll, Beijing 100021, Peoples R China
[5] Hunan Univ, Mol Sci & Biomed Lab, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[6] Echo Biotech Co Ltd, Beijing 102206, Peoples R China
基金
中国国家自然科学基金;
关键词
Small cell lung cancer; Targeted therapy; Aptamer; HDLBP; Cell cycle; RIBOSOME-INACTIVATING PROTEIN; ARALIA-ELATA; VIGILIN; CARCINOMA; SELECTION; CYCLE;
D O I
10.1016/j.yexcr.2019.06.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Small cell lung cancer (SCLC) has been a recalcitrant cancer without significant breakthroughs in clinical treatment during the past three decades. As there is a lack of effective protein inhibitor for SCLC targeted therapy, the discovery of new druggable SCLC biomarkers is a pressing work. Here we identified a new protein biomarker of SCLC, which is high density lipoprotein binding protein (HDLBP), through the aptamer generated by cell-SELEX against SCLC cells. Immunohistochemistry results showed an elevated HDLBP level in SCLC tissues from clinical samples. Attenuating HDLBP expression with siRNA inhibited proliferation and metastasis of SCLC cells in vitro and tumor formation in vivo. Mechanism study revealed the new function of HDLBP in promoting G1/S cell cycle transition for tumor progression. While the inhibitor of HDLBP has been reported, our work suggested a promising potential of targeting HDLBP to improve the treatment of fatal SCLC and a powerful tool of using cell-SELEX in cancer medicine.
引用
收藏
页数:8
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