Guo Yun-Wei, Wen Zhuo-Fu, Zheng Feng-Ping, Li Yong-Wei, Feng Zhi-Ying
Department of Gastroenterology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510630, PR China.
Ai Zheng. 2008 Apr;27(4):369-73.
BACKGROUND & OBJECTIVE: A proliferation-inducing ligand (APRIL), a new member of the tumor necrosis factor (TNF) family, can stimulate tumor cell growth and proliferation both in vitro and in vivo. This research was to detect the expression of APRIL in colorectal carcinoma tissues, and to compare the effects of 5-fluorouracil (5-FU) and cisplatin (DDP) on the expression of APRIL in colorectal carcinoma SW480 cells.
The protein and mRNA levels of APRIL in 56 specimens of human colorectal carcinoma and para-tumor tissues and in SW480 cells were determined by immunohistochemistry and real-time fluorescence quantitative reverse transcription-polymerase chain reaction (FQ-RT-PCR). SW480 cells were treated with 5-FU and DDP at various concentrations for 24 h, 48 h and 72 h. The changes of APRIL mRNA level were analyzed by FQ-RT-PCR.
Both positive rate and mRNA level of APRIL were significantly higher in colorectal carcinoma tissues than in para-tumor tissues (76.8% vs. 16.1%, 0.16+/-0.05 vs. 0.71+/-0.08, both P<0.001). The expression of APRIL was strong in SW480 cells. When treated with different concentrations of 5-FU, the mRNA level of APRIL in SW480 cells raised gradually and reached the highest levels at 72 h after treatment (0.85+/-0.10, 0.81+/-0.09, 0.83+/-0.11, and 0.90+/-0.12 at the concentrations of 25, 50, 100 and 200 microg/mL, respectively), which were significantly higher than those in blank control group (P<0.001). When treated with different concentrations of DDP, the mRNA level of APRIL in SW480 cells did not increase when compared with that in control group (P>0.05). After 72-hour treatment, the mRNA level of APRIL in SW480 cells was significantly lower in 10 microg/mL and 20 microg/mL DDP groups than in blank control group (0.44+/-0.05 and 0.40+/-0.07 vs. 0.57+/-0.06, P<0.05).
APRIL may promote the development of colorectal carcinoma. When chemotherapy is conducted to treat colorectal carcinoma, especially when 5-FU is included in the regimen, anti-APRIL therapy might be an important assistant treatment to counter the impact of APRIL caused by antitumor drugs.
增殖诱导配体(APRIL)是肿瘤坏死因子(TNF)家族的新成员,在体外和体内均可刺激肿瘤细胞生长和增殖。本研究旨在检测APRIL在结直肠癌组织中的表达,并比较5-氟尿嘧啶(5-FU)和顺铂(DDP)对结直肠癌SW480细胞中APRIL表达的影响。
采用免疫组织化学和实时荧光定量逆转录聚合酶链反应(FQ-RT-PCR)检测56例人结直肠癌及癌旁组织标本和SW480细胞中APRIL的蛋白和mRNA水平。将SW480细胞分别用不同浓度的5-FU和DDP处理24小时、48小时和72小时。通过FQ-RT-PCR分析APRIL mRNA水平的变化。
结直肠癌组织中APRIL的阳性率和mRNA水平均显著高于癌旁组织(分别为76.8%对16.1%,0.16±0.05对0.71±0.08,P均<0.001)。APRIL在SW(此处原文有误,应为SW)480细胞中表达较强。用不同浓度的5-FU处理后,SW480细胞中APRIL的mRNA水平逐渐升高,并在处理后72小时达到最高水平(25、50、100和200μg/mL浓度时分别为0.85±0.10、0.81±...(此处原文有缺失),均显著高于空白对照组(P<0.001)。用不同浓度的DDP处理后,SW480细胞中APRIL的mRNA水平与对照组相比无增加(P>0.05)。处理72小时后,10μg/mL和20μg/mL DDP组SW480细胞中APRIL的mRNA水平显著低于空白对照组(0.44±0.05和0.40±0.07对0.57±0.06,P<0.05)。
APRIL可能促进结直肠癌的发展。在对结直肠癌进行化疗时,尤其是化疗方案中包含5-FU时,抗APRIL治疗可能是对抗抗肿瘤药物引起的APRIL影响的重要辅助治疗手段。