DENG Li,ZHANG Xuan-zhen,WANG Wei-dong,CHEN Zheng-tang,CAO Zheng-huai.Recombinant human endostatin combined with paclitaxel-cisplatin chemotherapy in treatment of human breast cancer xenograft in nude mice[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(09):783-786.
DENG Li,ZHANG Xuan-zhen,WANG Wei-dong,CHEN Zheng-tang,CAO Zheng-huai.Recombinant human endostatin combined with paclitaxel-cisplatin chemotherapy in treatment of human breast cancer xenograft in nude mice[J].J Amry Med Univ (J Third Mil Med Univ),2008,30(09):783-786.DOI:
Objective To investigate the anti-angiogenesis and tumor inhibitory effects of recombinant human endostatin (rhES) combined with paclitaxel-cisplatin chemotherapy (TP regimen) on xenograft tumors in nude mice of human breast carcinoma cell MCF-7. Methods Forty-eight xenograft nude mice were randomized into group A and group B,then every group were divided 4 subgroups
that is
TP group (cisplatin 20 mg/kg at days 1
7 and 14
and paclitaxel 5
mg/kg at days 1 and 7
i.p.)
rhES group (rhES 10 mg·kg
-1
·d
-1
for 14 d
i.v.)
rhES+TP group (combined treatment as abovementioned)
and control group (normal saline
i.v.). Inhibitory rate of xenograft and tumor growth curve was calculated and plotted. Serum VEGF level was determined by ELISA
microvessel density (MVD) in tumors was measured by immunohistochemistry
and cell apoptosis was examined by TUNEL staining. Survival time was observed in group B. Results Serum VEGF and MVD was significantly lower in rhES+TP group than in other groups (P0.05)
but its apoptosis index was higher (P0.05). Survival time had no difference in rhES+TP group than in TP group
but was longer than that of control group (P0.05). Conclusion rhES combined TP regimen is better than TP regimen in tumor growth and microvessel growth of human breast cancer xenograft
but the survival is not significant prolonged within one treatment cycle.