|Table of Contents|

The expression levels and biological function of LRP1 in lung cancer cells

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2024 19
Page:
3643-3647
Research Field:
Publishing date:

Info

Title:
The expression levels and biological function of LRP1 in lung cancer cells
Author(s):
WANG HaiqiangZHANG TianyiZHANG WeifengYIN XunliangZHOU Yong'anZHAO Zhengwei
Department of Thoracic Surgery,the Second Affiliated Hospital of Air Force Medical University,Shaanxi Xi'an 710038,China.
Keywords:
lung cancerA549 cellsLRP1proliferationmigrationinvasion
PACS:
R734.2
DOI:
10.3969/j.issn.1672-4992.2024.19.003
Abstract:
Objective:To explore the expression levels and biological significance of low density lipoprotein receptor-related protein 1(LRP1) in lung cancer cells.Methods:Conventional culture of human lung cancer A549 cells,and RT-PCR method to detect the mRNA level of LRP1 in A549 cells.To construct siRNA infected cells targeting LRP1,using green fluorescent labeling vectors,observe infection efficiency through fluorescence microscopy,detect knockdown efficiency using RT-PCR,and detect changes in LRP1 expression levels using Western blot.A549/LRP1 siRNA cell lines were selected for functional experiments,and CCK-8 assay was used to detect changes in cell proliferation ability,scratch assay was used to detect changes in cell migration ability,and Transwell invasion chamber assay was used to detect changes in cell invasion ability.Results:From the quantitative PCR results,it can be seen that in A549 cells,compared to the NC group,the LRP1 gene knockout efficiency in the KD group was 77.7%.The mRNA level of LRP1 in the KD group cells was significantly lower than that in the NC group,and the difference was statistically significant(P<0.05).Western blot analysis showed that the expression level of LRP1 in the KD group was significantly downregulated compared to the NC group.The CCK-8 detection results showed that compared to the NC group,the KD group had a significant decrease in cell proliferation multiple on Day 5,and the difference was statistically significant(P<0.05).The scratch experiment results showed that compared with the NC group,the KD group showed a significant decrease in cell migration rates after 8 and 24 hours of scratch,with statistical significance(P<0.05).The results of Transwell invasion experiment showed that the invasion and metastasis rate of KD group cells significantly decreased after 24 hours of incubation in the invasion chamber,and the difference was statistically significant(P<0.05).Conclusion:LRP1 plays an important role in the biological function of lung cancer A549 cells.Downregulation of LRP1 can inhibit the proliferation,migration,and invasion ability of A549 cells.The research on the upstream and downstream signaling pathways of LRP1 molecule has certain clinical reference value in the diagnosis and treatment of lung cancer.

References:

[1]郑荣寿,陈茹,赫捷,等.2022年中国恶性肿瘤流行情况分析[J].中华肿瘤杂志,2024,46(3):221-231. ZHENG Rongshou,CHEN Ru,HE Jie,et al.Analysis of the epidemic of malignant tumors in China in 2022[J].Chinese Journal of Oncology,2024,46(3):221-231.
[2]HINTZE J,TOPAKTAS A,JEBARI S,et al.Functions of LDLR-related protein 1(LRP1) O-glycosylation[J].Glycobiology,2022,32(11):1048.
[3]T MARVIAN A,STAMELOUM,HOEGLINGER GU.LRP1:A novel mediator of tau uptake[J].Movement Disord,2020,35(7):1136.
[4]李若,田艳艳,高勇,等.应用RNAi技术沉默大转录本基因LRP1B[J].遗传,2009,31(1):36-42. LI Ruo,TIAN Yanyan,GAO Yong,et al.Applying RNAi technology to silence the large transcript gene LRP1B[J].Genetics,2009,31(1):36-42.
[5]DENG N,LIM,SHEN D,et al.LRP1 receptor-mediated immunosuppression of alpha-MMC on monocytes[J].Int Immunopharmacol,2019,70:80-87.
[6]PEIPEI XING,ZHICHAO LIAO,ZHIWU REN,et al.Roles of low-density lipoprotein receptor-related protein 1 intumors[J].Chinese Journal of Cancer,2016(1):24-32.
[7]朱萌瑛,沈浩,汪碧丽,等.LRP1在消化系统恶性肿瘤侵袭和预后中的调节作用[J].浙江临床医学,2024,26(1):13-16. ZHU Mengying,SHEN Hao,WANG Bili,et al.The regulatory role of LRP1 in the invasion and prognosis of malignant tumors in the digestive system[J].Zhejiang Clinical Medicine,2024,26(1):13-16
[8]RUAN H,CHAI Z,SHEN Q,et al.A novel peptide ligand RAP12 of LRP1 for glioma targeted drug delivery[J].Journal of Controlled Release,2018,279:306-315.
[9]刘磊,任明永,成荣杰,等.LRP1B在宫颈鳞癌中的表达与意义[J].中国妇幼健康研究,2017,28(5):495-497,516. LIU Lei,REN Mingyong,CHENG Rongjie,et al.The expression and significance of LRP1B in cervical squamous cell carcinoma[J].China Maternal and Child Health Research,2017,28(5):495-497,516
[10]KOHARA Y,HARAGUCHI R,KITAZAWA R,et al.Knockdown of LRP1 in RAW264 cells inhibits osteoclast differentiation and osteoclast-osteoblast interactions in vitro[J].Biochem Bioph Res Commun,2020,523(4):961-965.
[11]TIAN Y,WANG C,CHEN S,et al.Extracellular Hsp90 alpha and clusterin synergistically promote breast cancer epithelial-to-mesenchymal transition and metastasis via LRP1[J].J Cell Sci,2019,132(15):s228213.
[12]邓荣华.LRP1B在人胰腺癌细胞中的表达及其意义[D].衡阳:南华大学,2012. DENG Ronghua.Expression and significance of LRP1B in human pancreatic cancer cells[D].Hengyang:South China University,2012.
[13]HE M,CHEN GA,ZHANG XJ,et al.Stromal LRP1 in lung adenocarcinoma predicts clinical outcome[J].Clinical Cancer Research,2011,17(8):2426-2433.
[14]邢培培.骨肉瘤中LRP1-SNRNP25融合基因促进肿瘤细胞侵袭迁移的分子机制[D].天津:天津医科大学,2019. XING Peipei.The molecular mechanism of LRP1-SNRNP25 fusion gene promoting tumor cell invasion and migration in osteosarcoma[D].Tianjin:Tianjin Medical University,2019.
[15]熊瀚.基于ChinaPca全基因组数据和基因表达量探讨LRP1与前列腺癌的关系[D].南宁:广西医科大学,2019. XIONG Han.Exploring the relationship between LRP1 and prostate cancer based on ChinaPca whole genome data and gene expression levels[D].Nanning:Guangxi Medical University,2019.
[16]熊慧姊.YAP通过激活LRP1启动子促进黑色素瘤的发生发展[D].苏州:苏州大学,2016. XIONG Huizi.YAP promotes the occurrence and development of melanoma by activating the LRP1 promoter[D].Suzhou:Suzhou University,2016.
[17]张淑荣.基于Hsp90与LRP-1的SRL-PFAC方法建立及多肽筛选[D].长春:吉林大学,2020. ZHANG Shurong .Establishment of SRL-PFAC method and peptide screening based on Hsp90 and LRP-1[D].Changchun:Jilin University,2020.
[18]SNIGIREVA AV,VRUBLEVSKAYA VV,ZHMURINA MA,et al.The mechanisms of stimulation of migration and invasion of tumor cells by extracellular heat shock protein 90(eHsp90) in vitro[J].Biophysics,2018,63(6):931-939.
[19]WONG DS,JAY DG.Emerging roles of extracellular Hsp90 in cancer[J].Advances in Cancer Research,2016,130:141-164.

Memo

Memo:
National Natural Science Foundation of China(No.81402411);国家自然科学基金资助项目(编号:81402411)
Last Update: 2024-08-30