Tavares-Carreón Faviola, De la Torre-Zavala Susana, Arocha-Garza Hector Fernando, Souza Valeria, Galán-Wong Luis J, Avilés-Arnaut Hamlet
Facultad de Ciencias Biológicas, Instituto de Biotecnología, Universidad Autónoma de Nuevo León, San Nicolás de los Garza, Nuevo León, Mexico.
Departamento de Ecología Evolutiva, Instituto de Ecología, Universidad Nacional Autónoma de México, Coyoacán, Mexico.
PeerJ. 2020 Mar 12;8:e8686. doi: 10.7717/peerj.8686. eCollection 2020.
With the purpose of discovering new anticancer molecules that might have fewer side effects or reduce resistance to current antitumor drugs, a bioprospecting study of the microalgae of the Cuatro Cienegas Basin (CCB), an oasis in the Chihuahuan desert in Mexico was conducted. A microalgae was identified as sp. through sequencing the gene and reconstruction of a phylogenetic tree, and its anticancer activities were assessed using various in vitro assays and different cell lines of human cancers, including lung, skin melanoma, colorectal, breast and prostatic cancers, as well as a normal cell line. The values of IC of the microalgae methanolic extract using the MTT assay were lower than 20 μg/ml, except that in the lung cancer line and the normal cell line. In vitro, the microalgae extract caused the loss of membrane integrity, monitored by the trypan blue exclusion test and exhibited marked inhibition of adhesion and cell proliferation in cancer cell lines, through the evaluation of the clonogenic assay. Also, typical nuclear changes of apoptotic processes were observed under the microscope, using the dual acridine orange/ethidium bromide fluorescent staining. Finally, the microalgae extract increased the activity of caspases 3 and 7 in skin melanoma, colon, breast and prostate cancer cells, in the same way as the apoptotic inductor and powerful antitumoral drug, doxorubicin. This study shows the anticancer activity from sp., a microalgae isolated from the CCB.
为了发现可能副作用更少或能降低对当前抗肿瘤药物耐药性的新型抗癌分子,对位于墨西哥奇瓦瓦沙漠中的绿洲——夸特罗谢内加斯盆地(CCB)的微藻进行了生物勘探研究。通过对基因进行测序并重建系统发育树,将一种微藻鉴定为 sp.,并使用各种体外试验以及包括肺癌、皮肤黑色素瘤、结直肠癌、乳腺癌和前列腺癌在内的多种人类癌症细胞系以及一种正常细胞系评估了其抗癌活性。除肺癌细胞系和正常细胞系外,使用MTT 法测得的该微藻甲醇提取物的半数抑制浓度(IC)值低于20μg/ml。在体外,通过台盼蓝排斥试验监测发现该微藻提取物导致细胞膜完整性丧失,并且通过克隆形成试验评估显示,其对癌细胞系的黏附及细胞增殖具有显著抑制作用。此外,使用双吖啶橙/溴化乙锭荧光染色在显微镜下观察到了凋亡过程中典型的细胞核变化。最后,该微藻提取物增加了皮肤黑色素瘤、结肠癌、乳腺癌和前列腺癌细胞中半胱天冬酶3和7的活性,其作用方式与凋亡诱导剂及强效抗肿瘤药物阿霉素相同。这项研究显示了从CCB分离出的一种微藻 sp. 的抗癌活性。