| Literature DB >> 29712537 |
Yan Mei1, Jun-Ping Yang1, Yan-Hong Lang1, Li-Xia Peng1, Ming-Ming Yang2, Qing Liu2, Dong-Fang Meng1, Li-Sheng Zheng1, Yuan-Yuan Qiang1, Liang Xu1, Chang-Zhi Li1, Wen-Wen Wei1, Ting Niu2, Xing-Si Peng1, Qin Yang1, Fen Lin1, Hao Hu3, Hong-Fa Xu4, Bi-Jun Huang1, Li-Jing Wang2, Chao-Nan Qian1,5.
Abstract
It is believed that the alteration of tissue microenvironment would affect cancer initiation and progression. However, little is known in terms of the underlying molecular mechanisms that would affect the initiation and progression of breast cancer. In the present study, we use two murine mammary tumor models with different speeds of tumor initiation and progression for whole genome expression profiling to reveal the involved genes and signaling pathways. The pathways regulating PI3K-Akt signaling and Ras signaling were activated in Fvb mice and promoted tumor progression. Contrastingly, the pathways regulating apoptosis and cellular senescence were activated in Fvb.B6 mice and suppressed tumor progression. We identified distinct patterns of oncogenic pathways activation at different stages of breast cancer, and uncovered five oncogenic pathways that were activated in both human and mouse breast cancers. The genes and pathways discovered in our study would be useful information for other researchers and drug development.Entities:
Keywords: Apoptosis; Breast cancer; Cancer progression; PI3K-Akt signaling; RNA-sequencing; Ras signaling
Mesh:
Year: 2018 PMID: 29712537 PMCID: PMC6103659 DOI: 10.1080/15384101.2018.1442629
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534