2003•Zhongliu fangzhi yanjiuRequires access

Relationship between PCNA expression and apoptosis of human lung cancer cell line

Xiaorong Dong, Liu Li, Jihua Dong

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Abstract

Objective To investigate the relationship between proliferating cell nuclear antigen (PCNA) expression and apoptosis of human lung cancer cell line.Methods Arsenic trioxide (As_2O_3) was used to induce the direct apoptosis in human lung cancer GLC-82 cell line. The MTT method and flowcytometry (FCM) were used for detection. With RT-PCR, the changes and relations of PCNA in the process of GLC-82 apoptosis were studied. Results The data showed that As_2O_3 significatly. inhibited proliferation of GLC-82 cells and inhibiting effects had a dose-and time-dependence. The change of DNA content of GLC-82 cell indicated that cell cycle progress could be blocked by As_2O_3 in G_2/M phase, with apperence of sub-G_1 peak in dose-dependent manner.And PCNA mRNA activation was inhibited by As_2O_3. Conclusion During apoptosis of GLC-82 cell induced by As_2O_3,PCNA activation could apparently be inhibited. Hence,inhibition of PCNA activation may represent a new chemosensitisation for tumors resistant to anticancer drugs.

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Objective To investigate the relationship between proliferating cell nuclear antigen (PCNA) expression and apoptosis of human lung cancer cell line.Methods Arsenic trioxide (As_2O_3) was used to induce the direct apoptosis in human lung cancer GLC-82 cell line. The MTT method and flowcytometry (FCM) were used for detection. With RT-PCR, the changes and relations of PCNA in the process of GLC-82 apoptosis were studied. Results The data showed that As_2O_3 significatly. inhibited proliferation of GLC-82 cells and inhibiting effects had a dose-and time-dependence. The change of DNA content of GLC-82 cell indicated that cell cycle progress could be blocked by As_2O_3 in G_2/M phase, with apperence of sub-G_1 peak in dose-dependent manner.And PCNA mRNA activation was inhibited by As_2O_3. Conclusion During apoptosis of GLC-82 cell induced by As_2O_3,PCNA activation could apparently be inhibited. Hence,inhibition of PCNA activation may represent a new chemosensitisation for tumors resistant to anticancer drugs.

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Available abstract

Objective To investigate the relationship between proliferating cell nuclear antigen (PCNA) expression and apoptosis of human lung cancer cell line.Methods Arsenic trioxide (As_2O_3) was used to induce the direct apoptosis in human lung cancer GLC-82 cell line. The MTT method and flowcytometry (FCM) were used for detection. With RT-PCR, the changes and relations of PCNA in the process of GLC-82 apoptosis were studied. Results The data showed that As_2O_3 significatly. inhibited proliferation of GLC-82 cells and inhibiting effects had a dose-and time-dependence. The change of DNA content of GLC-82 cell indicated that cell cycle progress could be blocked by As_2O_3 in G_2/M phase, with apperence of sub-G_1 peak in dose-dependent manner.And PCNA mRNA activation was inhibited by As_2O_3. Conclusion During apoptosis of GLC-82 cell induced by As_2O_3,PCNA activation could apparently be inhibited. Hence,inhibition of PCNA activation may represent a new chemosensitisation for tumors resistant to anticancer drugs.

Key concepts: Proliferating cell nuclear antigen, Apoptosis, Arsenic trioxide, Cell cycle, Molecular biology, Chemistry, Cell growth, Lung cancer

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