Antheraea proylei J. Sericin Induces Apoptosis in a Caspase-Dependent Manner in A549 and HeLa Cells

赫拉 细胞凋亡 丝胶 细胞生物学 化学 A549电池 半胱氨酸蛋白酶 分子生物学 生物 细胞 材料科学 程序性细胞死亡 生物化学 丝绸 复合材料
作者
Potsangbam Jolly Devi,Asem Robinson Singh,Naorem Tarundas Singh,Laishram Rupachandra Singh,Sanjenbam Kunjeshwori Devi,Lisam Shanjukumar Singh
出处
期刊:Anti-cancer Agents in Medicinal Chemistry [Bentham Science Publishers]
卷期号:23 被引量:1
标识
DOI:10.2174/1871520623666230329123437
摘要

Background:: In spite of much progress in cancer, the global cancer burden is still significant and increasing. Sericin, an adhesive protein of silk cocoons, has been shown to be a potential protein in various biomedical applications, including cancer therapeutics. The present study evaluates the anticancer property of sericin from cocoons of Antheraea proylei J (SAP) against human lung cancer (A549) and cervical cancer (HeLa) cell lines. This is the first report of anti-cancer activity of the non-mulberry silkworm A. proylei J. Objective:: Establish the antiproliferative potential of SAP. 2. Identify the molecular mechanism of cell death induced by SAP on two different cell lines Aims:: To investigate the anticancer activity of sericin preparation from cocoons of A. proylei. Methods:: SAP was prepared from cocoons of A. proylei J. by the process of the degumming method. Cytotoxic activity was assessed by MTT assay, and genotoxicity was assessed by comet assay. Cleavage of caspase and PARP proteins and phosphorylation of MAPK pathway members were analysed by Western blotting. Cell cycle analysis was done by flow cytometer. Results:: SAP causes cytotoxicity to A549 and HeLa cell lines with the IC50 values 3.8 and 3.9 μg/μl respectively. SAP induces apoptosis in a dose-dependent manner through caspase-3 and p38, MAPK pathways in A549 and HeLa cells. Moreover, in A549 and HeLa cells, SAP induces cell cycle arrest at the S phase in a dose-dependent manner. Conclusion:: The difference in the molecular mechanisms of apoptosis induced by SAP in A549 and HeLa cell lines may be due to the difference in the genotypes of the cancer cell lines. However, further investigation is warranted. The overall results of the present study envisage the possibility of using SAP as an anti-tumorigenic agent.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
科研通AI6应助科研通管家采纳,获得10
刚刚
桐桐应助科研通管家采纳,获得10
刚刚
wanci应助科研通管家采纳,获得10
刚刚
桐桐应助科研通管家采纳,获得10
1秒前
浮游应助科研通管家采纳,获得10
1秒前
zcl应助科研通管家采纳,获得200
1秒前
乐乐应助科研通管家采纳,获得10
1秒前
浮游应助科研通管家采纳,获得10
1秒前
科研通AI6应助科研通管家采纳,获得10
1秒前
浮游应助科研通管家采纳,获得10
1秒前
科研通AI5应助科研通管家采纳,获得10
1秒前
慕青应助科研通管家采纳,获得10
1秒前
斯文败类应助科研通管家采纳,获得10
2秒前
Zx_1993应助科研通管家采纳,获得10
2秒前
科研通AI6应助科研通管家采纳,获得10
2秒前
英俊的铭应助科研通管家采纳,获得10
2秒前
2秒前
wanci应助科研通管家采纳,获得150
2秒前
浮游应助科研通管家采纳,获得10
2秒前
浮游应助wang1030采纳,获得30
2秒前
zcl应助科研通管家采纳,获得150
2秒前
okeljy发布了新的文献求助10
2秒前
2秒前
刘刘完成签到 ,获得积分10
2秒前
bai完成签到,获得积分10
3秒前
WZQ发布了新的文献求助10
4秒前
千早爱音完成签到,获得积分10
5秒前
5秒前
6秒前
whz完成签到,获得积分10
6秒前
小飞飞发布了新的文献求助10
7秒前
华仔应助vz采纳,获得10
8秒前
yuanshuai发布了新的文献求助10
10秒前
Elm完成签到,获得积分10
10秒前
xixixiziwei完成签到,获得积分10
10秒前
Dawn完成签到,获得积分10
12秒前
清爽凝阳发布了新的文献求助10
12秒前
量子星尘发布了新的文献求助10
14秒前
15秒前
zgaolei发布了新的文献求助10
16秒前
高分求助中
Comprehensive Toxicology Fourth Edition 24000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
LRZ Gitlab附件(3D Matching of TerraSAR-X Derived Ground Control Points to Mobile Mapping Data 附件) 2000
Pipeline and riser loss of containment 2001 - 2020 (PARLOC 2020) 1000
World Nuclear Fuel Report: Global Scenarios for Demand and Supply Availability 2025-2040 800
Handbook of Social and Emotional Learning 800
Risankizumab Versus Ustekinumab For Patients with Moderate to Severe Crohn's Disease: Results from the Phase 3B SEQUENCE Study 600
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 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 5133576
求助须知:如何正确求助?哪些是违规求助? 4334702
关于积分的说明 13504381
捐赠科研通 4171698
什么是DOI,文献DOI怎么找? 2287273
邀请新用户注册赠送积分活动 1288197
关于科研通互助平台的介绍 1229045