Department of Pathology, Kunshan First People's Hospital Affiliated to Jiangsu University, Kunshan, Jiangsu, 215004, People's Republic of China.
Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu, 215004, People's Republic of China.
BMC Cancer. 2019 Jun 17;19(1):589. doi: 10.1186/s12885-019-5791-1.
Numerous studies have explored the anti-tumor effect of berberine (BBR), but little clinical evidence guides the use of BBR in cancer patients.
Our aim was to investigate the impact of BBR on various cancers in healthy animals to promote the transformation from bench to bed.
PubMed, Embase, Springer, and Cochrane databases were searched from January 2000 to October 2018 for relevant articles.
Only published studies focusing on the relationship between BBR and various cancers in vivo were qualified. Two review authors independently assessed the risk of bias for each study, and any disagreement was resolved by discussion or by involving a third assessor.
A total of 26 studies from 2000 to 2018, focusing on various cancer types, including breast cancer, liver cancer, colorectal cancer, nasopharyngeal carcinoma, lung cancer, gastric cancer, neuroepithelial cancer, endometrial carcinoma, esophageal cancer, tongue cancer, cholangiocarcinoma, and sarcoma were included. Overall, BBR reduced tumor volume (SMD =3.72, 95% CI: 2.89, 4.56, Z = 8.73, p < 0.00001) and tumor weight (SMD =2.35, 95% CI: 1.51, 3.19, Z = 5.50, p < 0.00001) in a linear The dose-response relationship (Pearson r = - 0.6717, p < 0.0001 in tumor volume analysis; Pearson r = - 0.7704, p < 0.0005 in tumor weight analysis). BBR inhibited angiogenesis in tumor tissues (SMD = 4.29, 95% CI: 2.14, 6.44, Z = 3.92, p < 0.00001), but it had no significant effect on the body weight of experimental animals (SMD = 0.11, 95% CI: - 0.70, 0.92, Z = 0.27, p = 0.78). Publication bias was not detected.
BBR exerted anti-tumor effects in a variety of tumors in vivo, especially breast cancer and lung cancer, and the evidence was still insufficient in colorectal cancer and gastric cancer.
已有大量研究探讨了小檗碱(BBR)的抗肿瘤作用,但很少有临床证据指导癌症患者使用 BBR。
我们旨在研究 BBR 对健康动物各种癌症的影响,以促进从基础研究到临床应用的转化。
从 2000 年 1 月至 2018 年 10 月,我们在 PubMed、Embase、Springer 和 Cochrane 数据库中检索了相关文献。
只有聚焦于体内 BBR 与各种癌症之间关系的已发表研究才符合纳入标准。两位综述作者独立评估了每项研究的偏倚风险,如果存在分歧,则通过讨论或请第三位评估员解决。
共纳入了 2000 年至 2018 年的 26 项研究,涵盖了多种癌症类型,包括乳腺癌、肝癌、结直肠癌、鼻咽癌、肺癌、胃癌、神经上皮癌、子宫内膜癌、食管癌、舌癌、胆管癌和肉瘤。总体而言,BBR 可降低肿瘤体积(SMD=3.72,95%CI:2.89,4.56,Z=8.73,p<0.00001)和肿瘤重量(SMD=2.35,95%CI:1.51,3.19,Z=5.50,p<0.00001),呈线性剂量-反应关系(肿瘤体积分析的 Pearson r=-0.6717,p<0.0001;肿瘤重量分析的 Pearson r=-0.7704,p<0.0005)。BBR 抑制肿瘤组织中的血管生成(SMD=4.29,95%CI:2.14,6.44,Z=3.92,p<0.00001),但对实验动物的体重无显著影响(SMD=0.11,95%CI:-0.70,0.92,Z=0.27,p=0.78)。未检测到发表偏倚。
BBR 在体内多种肿瘤中发挥抗肿瘤作用,特别是乳腺癌和肺癌,而在结直肠癌和胃癌中的证据仍不足。