Sakakura C, Sweeney E A, Shirahama T, Igarashi Y, Hakomori S, Tsujimoto H, Imanishi T, Ogaki M, Ohyama T, Yamazaki J, Hagiwara A, Yamaguchi T, Sawai K, Takahashi T
Biomembrane Institute, Seattle, WA 98119, USA.
Surg Today. 1997;27(7):676-9. doi: 10.1007/BF02388231.
Bax, one of the bcl-2 family genes, is expressed in a number of untransformed cell lines and various breast tissues, whereas only weak or no expression has been detected in breast cancer cell lines and malignant breast tissue. Human breast cancer MCF-7 cells, which have a weak bax gene expression, were stably transfected with pCX2neo bax, encoding human bax; and two unique clones, MCF-7/bax-1 and MCF-7/ bax-2, that expressed different levels of bax were generated. Sensitivity to cisplatin (CDDP) and etoposide (VP-16) was examined and each stable transfectant was more sensitive to these agents than the parental MCF-7 cells. The degree of enhancement in sensitivity to these anticancer agents was dependent on the expression level of bax. The enzyme-linked immunosorbent assay (ELISA), which quantifies DNA damage, demonstrated that this sensitization was due to apoptosis. Thus, we suggest that exogenous bax-alpha overexpression may be one of the factors determining cellular chemosensitivity in MCF-7 breast cancer cells and that it could be applied therapeutically to enhance chemosensitivity in breast cancer cells.
Bax是bcl-2家族基因之一,在许多未转化的细胞系和各种乳腺组织中表达,而在乳腺癌细胞系和恶性乳腺组织中仅检测到微弱表达或无表达。人乳腺癌MCF-7细胞系中bax基因表达较弱,用编码人Bax的pCX2neo bax进行稳定转染;并产生了两个表达不同水平Bax的独特克隆,即MCF-7/bax-1和MCF-7/bax-2。检测了它们对顺铂(CDDP)和依托泊苷(VP-16)的敏感性,每个稳定转染子对这些药物的敏感性均高于亲本MCF-7细胞。对这些抗癌药物敏感性增强的程度取决于Bax的表达水平。定量DNA损伤的酶联免疫吸附测定(ELISA)表明,这种致敏作用是由于细胞凋亡所致。因此,我们认为外源性Bax-α过表达可能是决定MCF-7乳腺癌细胞化学敏感性的因素之一,并且它可用于治疗性增强乳腺癌细胞的化学敏感性。