2006•Di-Si Junyi Daxue xuebaoRequires access

Apoptosis-promoting effect of resveratrol combined with 5-FU on human breast cancer cell line MCF7

Ke Xing

Open publisher page 0 citations

Abstract

AIM: To investigate whether 5-FU in combination with resveratrol can accelerate the apoptosis of human breast cancer cell line MCF7 in vitro. METHODS: Four breast cancer cell lines (MCF7, MDA-MB-231, SK-BR-3 and Bcap-37) were incubated with different concentrations of resveratrol or/and 5-FU for 48 h, then cell survival rate was measured by MTT assay and cell morphological change was observed by phase contrast microscope. Apoptosis was detected by flow cytometry (Annexin V/PI staining) analysis and Hoechst33258 staining. RESULTS: Resveratrol could inhibit the growth of MCF7, MDA-MB-231, SK-BR-3 and Bcap-37 to different extents. The IC_ 50 values of resveratrol in MCF7, MDA-MB-231, SK-BR-3 and Bcap-37 cells were 65, 207, 139 and 213 μmol/L, respectively. The IC_ 50 value of 5-FU in MCF7 cells was 13 μmol/L. When 5-FU and 65 μmol/L resveratrol were combined, the IC_ 50 value of 5-FU in MCF7 cells was decreased to 9 μmol/L. Compared with the treatment with 13 μmol/L 5-FU or 65 μmol/L resveratrol alone, the percentage of Annexin V(+)/PI(-) MCF7 cells increased when these 2 drugs were used in combination. The number of apoptotic MCF7 cells calculated with flow cytometry was accordant with the result got with Hoechst33258 staining. CONCLUSION: Resveratrol interacts synergistically with 5-FU to induce the apoptosis of MCF7 cells, which suggests that resveratrol is a secondary chemotherapeutic medicine for treating breast cancer.

About this research paper

What this paper is about

AIM: To investigate whether 5-FU in combination with resveratrol can accelerate the apoptosis of human breast cancer cell line MCF7 in vitro. METHODS: Four breast cancer cell lines (MCF7, MDA-MB-231, SK-BR-3 and Bcap-37) were incubated with different concentrations of resveratrol or/and 5-FU for 48 h, then cell survival rate was measured by MTT assay and cell morphological change was observed by phase contrast microscope. Apoptosis was detected by flow cytometry (Annexin V/PI staining) analysis and Hoechst33258 staining. RESULTS: Resveratrol could inhibit the growth of MCF7, MDA-MB-231, SK-BR-3 and Bcap-37 to different extents. The IC_ 50 values of resveratrol in MCF7, MDA-MB-231, SK-BR-3 and Bcap-37 cells were 65, 207, 139 and 213 μmol/L, respectively. The IC_ 50 value of 5-FU in MCF7 cells was 13 μmol/L. When 5-FU and 65 μmol/L resveratrol were combined, the IC_ 50 value of 5-FU in MCF7 cells was decreased to 9 μmol/L. Compared with the treatment with 13 μmol/L 5-FU or 65 μmol/L resveratrol alone, the percentage of Annexin V(+)/PI(-) MCF7 cells increased when these 2 drugs were used in combination. The number of apoptotic MCF7 cells calculated with flow cytometry was accordant with the result got with Hoechst33258 staining. CONCLUSION: Resveratrol interacts synergistically with 5-FU to induce the apoptosis of MCF7 cells, which suggests that resveratrol is a secondary chemotherapeutic medicine for treating breast cancer.

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

AIM: To investigate whether 5-FU in combination with resveratrol can accelerate the apoptosis of human breast cancer cell line MCF7 in vitro. METHODS: Four breast cancer cell lines (MCF7, MDA-MB-231, SK-BR-3 and Bcap-37) were incubated with different concentrations of resveratrol or/and 5-FU for 48 h, then cell survival rate was measured by MTT assay and cell morphological change was observed by phase contrast microscope. Apoptosis was detected by flow cytometry (Annexin V/PI staining) analysis and Hoechst33258 staining. RESULTS: Resveratrol could inhibit the growth of MCF7, MDA-MB-231, SK-BR-3 and Bcap-37 to different extents. The IC_ 50 values of resveratrol in MCF7, MDA-MB-231, SK-BR-3 and Bcap-37 cells were 65, 207, 139 and 213 μmol/L, respectively. The IC_ 50 value of 5-FU in MCF7 cells was 13 μmol/L. When 5-FU and 65 μmol/L resveratrol were combined, the IC_ 50 value of 5-FU in MCF7 cells was decreased to 9 μmol/L. Compared with the treatment with 13 μmol/L 5-FU or 65 μmol/L resveratrol alone, the percentage of Annexin V(+)/PI(-) MCF7 cells increased when these 2 drugs were used in combination. The number of apoptotic MCF7 cells calculated with flow cytometry was accordant with the result got with Hoechst33258 staining. CONCLUSION: Resveratrol interacts synergistically with 5-FU to induce the apoptosis of MCF7 cells, which suggests that resveratrol is a secondary chemotherapeutic medicine for treating breast cancer.

Key concepts: Resveratrol, Annexin, Apoptosis, Flow cytometry, Molecular biology, MTT assay, Pi, Staining

Related papers

Back to paper searchBrowse research topicsOriginal source
Apoptosis-promoting effect of resveratrol combined with 5-FU on human breast cancer cell line MCF7 — Research Paper | ScholarLens