A signature for induced pluripotent stem cell-associated genes in colorectal cancer
Autor: | Yong-Xia Liu, Yu-hong Liu, Su Yao, Jianming Li, Hong-Mei Sui, Jun Zhou, Xun-Hua Liu, Ping Zheng, Zheng-Quan Xiao, Cheng Xing, Ying Li, Lin Chen |
---|---|
Rok vydání: | 2012 |
Předmět: |
Homeobox protein NANOG
Male Pluripotent Stem Cells Cancer Research Somatic cell Blotting Western Fluorescent Antibody Technique Biology LIN28 Disease-Free Survival Transcriptome SOX2 Humans RNA Messenger Induced pluripotent stem cell Neoplasm Staging Homeodomain Proteins Reverse Transcriptase Polymerase Chain Reaction Nanog Homeobox Protein RNA-Binding Proteins Hematology General Medicine Middle Aged Immunohistochemistry digestive system diseases Gene expression profiling Oncology Immunology Cancer research Female Colorectal Neoplasms Octamer Transcription Factor-3 |
Zdroj: | Medical oncology (Northwood, London, England). 30(1) |
ISSN: | 1559-131X |
Popis: | Genes associated with induced pluripotent stem cells (iPS genes) are several pivotal transcriptional factors, which are used to induce pluripotent stem cells from some adult somatic cells. The roles of these iPS genes and especially the signature for these iPS genes in colorectal cancer (CRC) are still unclear. Overexpressed Oct4 and Lin28 but down-regulated Nanog were found in tumor tissues compared with that in their paired normal counterparts of CRC patients. Interestingly, we found that Oct4, Lin28 and Nanog were highly overexpressed in some patients. And the signature for iPS genes was correlated with tumor site (P = 0.012), lymph node status (P = 0.033), Dukes classification (P = 0.033) of CRC patients. Moreover, an independent public expression profiling data showed signature for the four iPS genes could successfully be used to predict the survival of CRC patients with Dukes stages B and C. Immunofluorescent staining of fresh CRC tissues from patients showed that strong co-expressions of Oct4 and Nanog proteins or Sox2 and Lin28 were present in some CRC cells. Then, CRC cell subclone with four iPS genes overexpression were establish by a mixed retroviral system. We found that iPS genes promote sphere-formation, proliferation, colony formation, migration of human CRC cells in vitro and tumor growth in vivo. Our study first shows the clinical significance of iPS signature in CRC patients. |
Databáze: | OpenAIRE |
Externí odkaz: |