Abstract
Breast cancer is a common malignancy that severely threatens women's mental health and lives. The paclitaxel-resistant breast cancer cells were established through a continuous stimulation with paclitaxel in a stepwise escalating concentration manner. The expression of MAP7 was detected by RT-P CR and western blot. The annexin V staining assay was used to measure the cell apoptosis ratio. The expression of cell invasive ability and apoptosis-related proteins was detected by western blot assay. The cellular motility was tested via transwell and wound healing assays. This study indicated that the MAP7 expression was upregulated in breast cancer cells and paclitaxel-resistant breast cancer cells. Moreover, downregulating MAP7 not only suppressed cell viability, motility and invasion, but also enhanced cellular apoptosis in paclitaxel-resistant breast cancer cells. In summary, this study investigated the effect of MAP7 protein on cell critical physiological function, which provided a novel potential target for treating paclitaxel-resistant breast cancer.
Disclosure statement
The authors state that there are no conflicts of interest to disclose.
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
Authors contribution
Xiaoyan Wang and Xuezhen Cao designed the study, supervised the data collection; Youyi Wu analyzed the data, interpreted the data; Tingting Chen prepare the manuscript for publication and reviewed the draft of the manuscript. All authors have read and approved the manuscript.