Effect of the isoflavone corylin from cullen corylifolium on colorectal cancer growth, by targeting the STAT3 signaling pathway

生存素 活力测定 细胞凋亡 细胞生长 癌症研究 STAT蛋白 车站3 化学 生物 信号转导 生物化学 细胞生物学
作者
Lehe Yang,Yulei Yao,Ying Bai,Dandan Zheng,Feng Zhou,Luye Chen,Wanle Hu,Youqun Xiang,Jing Wang,Zhiguo Liu,Liangxing Wang,Xiaoying Huang,Chengguang Zhao
出处
期刊:Phytomedicine [Elsevier]
卷期号:80: 153366-153366 被引量:21
标识
DOI:10.1016/j.phymed.2020.153366
摘要

Colorectal cancer (CRC) is one of the most common cancers worldwide. Corylin is an isoflavone extracted from Cullen corylifolium (L.) Medik., which is widely used anti-inflammatory and anticancer in Asian countries. Signal transducer and activator of transcription 3 (STAT3) plays an important role in the occurrence and development of CRC. To analyze the antitumor activity of corylin in CRC and to elucidate its molecular mechanisms of action. The human CRC cell lines HCT116, RKO, and SW480 and immunodeficient mice were used as models to study the antitumor effect of corylin. The potent anti-proliferative, anti-migration and proapoptotic effects of corylin were observed by cell viability, colony formation assays, wound-healing migration assay, and cell apoptosis assay. Immunostaining analysis and western blot analysis revealed inhibition of the STAT3 signaling axis. We found that corylin could significantly reduce the viability and stimulate apoptosis in human CRC cells in a dose-dependent manner. Corylin decreased the expression levels of P-STAT3 and STAT3 target proteins, such as myeloid cell leukemia-1(MCL-1), Survivin, VEGF and B-cell lymphoma 2 (BCL-2). It also upregulated the expression levels of the proapoptotic proteins BCL-2-associated X protein (BAX) and Cl-caspase 3. Moreover, corylin reduced the nuclear localization of STAT3. Furthermore, corylin inhibited the growth of the tumor in CRC mouse models. Our findings provide convincing results that could support the role of corylin in the treatment of CRC through inhibiting the STAT3 pathway. It is conceivable that corylin should be further explored as a unique STAT3 inhibitor in antitumor therapy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ayu发布了新的文献求助10
刚刚
2秒前
彩色傲柏发布了新的文献求助10
2秒前
Orange应助滕达采纳,获得10
3秒前
好吃的蛋挞完成签到,获得积分10
4秒前
英姑应助俊逸的静竹采纳,获得10
4秒前
小牙医完成签到,获得积分10
5秒前
小蘑菇应助热心的语梦采纳,获得10
6秒前
开心夜云完成签到 ,获得积分10
7秒前
snackdragon完成签到 ,获得积分10
9秒前
可爱的函函应助Pec采纳,获得10
10秒前
xuanli完成签到,获得积分10
10秒前
宇宙暴龙战士暴打魔法少女完成签到,获得积分10
12秒前
坚定岂愈发布了新的文献求助10
12秒前
LELE完成签到 ,获得积分10
12秒前
JamesPei应助彩色傲柏采纳,获得10
13秒前
13秒前
搜集达人应助科研通管家采纳,获得10
14秒前
科研通AI2S应助科研通管家采纳,获得10
14秒前
wanci应助科研通管家采纳,获得10
15秒前
兔兔应助科研通管家采纳,获得10
15秒前
萧水白发布了新的文献求助100
15秒前
跳跃的电话完成签到,获得积分10
16秒前
ding应助Small-violet采纳,获得10
16秒前
17秒前
19秒前
八戒的梦想完成签到,获得积分10
19秒前
滕达发布了新的文献求助10
19秒前
briliian发布了新的文献求助10
21秒前
DaLu完成签到,获得积分10
22秒前
23秒前
23秒前
研友_V8Qmr8完成签到,获得积分10
26秒前
ZeradesY完成签到,获得积分10
26秒前
英姑应助寒冷乐驹采纳,获得30
26秒前
kohu完成签到,获得积分10
27秒前
研友_V8Qmr8发布了新的文献求助10
28秒前
30秒前
dagongren完成签到,获得积分10
30秒前
31秒前
高分求助中
Evolution 10000
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Foreign Policy of the French Second Empire: A Bibliography 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
China's Relations With Japan 1945-83: The Role of Liao Chengzhi 400
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3147946
求助须知:如何正确求助?哪些是违规求助? 2798939
关于积分的说明 7832669
捐赠科研通 2456017
什么是DOI,文献DOI怎么找? 1307045
科研通“疑难数据库(出版商)”最低求助积分说明 628043
版权声明 601620