2005•Acta Universitatis Medicinalis Secondae ShanghaiRequires access

Effect of B7-1 Costimulator Expression on Growth and Apoptosis of Lewis Lung Cancer

Zhiwei Chen, Huang Shaoguang, Meilin Liao, Wan Huan-ying

Open publisher page 0 citations

Abstract

Objective To investigate the effect of B7-1 expression on growth and apoptosis of Lewis lung cancer (LLC). Methods Eighteen mice with Lewis lung cancer were divided into 3 groups: control, blank control vector and B7-1 group. Two weeks later, the expression rates of B7-1 and CD8 + were determined, and apoptotic index (AI) were calculated. Results The B7-1 molecules expression rate of B7-1 group was (46.6±5.7)%, and AI of B7-1 group (5.3±1.0)%. They were higher than other groups (P0.05). The percent of CD8 + cells in the blood and spleen of B7-1 group was (15.4±3.2)% and (41.8±21.8)%, respectively, which were higher than other groups (P0.05). The tumor suppress rate of B7-1 group was 34.6% and 87.0% at d 8 and d 14, respectively. Conclusion Increase in the B7-1 expression of tumor can not only suppress tumor growth and induce apoptosis, but also can enhance immunogenicity.

About this research paper

What this paper is about

Objective To investigate the effect of B7-1 expression on growth and apoptosis of Lewis lung cancer (LLC). Methods Eighteen mice with Lewis lung cancer were divided into 3 groups: control, blank control vector and B7-1 group. Two weeks later, the expression rates of B7-1 and CD8 + were determined, and apoptotic index (AI) were calculated. Results The B7-1 molecules expression rate of B7-1 group was (46.6±5.7)%, and AI of B7-1 group (5.3±1.0)%. They were higher than other groups (P0.05). The percent of CD8 + cells in the blood and spleen of B7-1 group was (15.4±3.2)% and (41.8±21.8)%, respectively, which were higher than other groups (P0.05). The tumor suppress rate of B7-1 group was 34.6% and 87.0% at d 8 and d 14, respectively. Conclusion Increase in the B7-1 expression of tumor can not only suppress tumor growth and induce apoptosis, but also can enhance immunogenicity.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the effect of B7-1 expression on growth and apoptosis of Lewis lung cancer (LLC). Methods Eighteen mice with Lewis lung cancer were divided into 3 groups: control, blank control vector and B7-1 group. Two weeks later, the expression rates of B7-1 and CD8 + were determined, and apoptotic index (AI) were calculated. Results The B7-1 molecules expression rate of B7-1 group was (46.6±5.7)%, and AI of B7-1 group (5.3±1.0)%. They were higher than other groups (P0.05). The percent of CD8 + cells in the blood and spleen of B7-1 group was (15.4±3.2)% and (41.8±21.8)%, respectively, which were higher than other groups (P0.05). The tumor suppress rate of B7-1 group was 34.6% and 87.0% at d 8 and d 14, respectively. Conclusion Increase in the B7-1 expression of tumor can not only suppress tumor growth and induce apoptosis, but also can enhance immunogenicity.

Key concepts: Apoptosis, Immunogenicity, Lung cancer, CD8, Spleen, Cancer, Medicine, Cytotoxic T cell

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of B7-1 Costimulator Expression on Growth and Apoptosis of Lewis Lung Cancer — Research Paper | ScholarLens