TY - JOUR
T1 - Transcriptome analysis of CD133-positive stem cells and prognostic value of survivin in colorectal cancer
AU - Kim, Seung Tae
AU - Sohn, Insuk
AU - Do, In Gu
AU - Jang, Jiryeon
AU - Kim, Seok Hyung
AU - Jung, In Ho
AU - Park, Joon Oh
AU - Park, Young Suk
AU - Talasaz, Amirali
AU - Lee, Jeeyun
AU - Kim, Hee Cheol
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Background/Aim: CD133 is an important, but not exclusive, biomarker of colorectal cancer (CRC) stem cells. Materials and Methods: In order to identify other CRC stem cell-specific genes, we performed a comparative expression profiling of CD133+ and CD133- cell populations in primary and metastatic tumors from four patients with CRC. CD133+ and CD133- CRC cells were isolated using MagSweeper and used for whole-transcriptome analysis with RNA-Seq. Results: We found that in CD133+ cells, 17 genes (RNASE2, PRB2, IL4, MGC27382, CLEC4C, SALL3, GIMAP1, ISG15, LOC728875, ZIK1, ICAM2, CCDC7, CDYL2, LRRC2, ZEB1, OSTF1 and CCDC144B) were significantly up-regulated compared to CD133- CRC cells. Among them, IL4 has been known as an inducer of survivin implicated in the survival and proliferation of cancer cells. However, the prognostic value of survivin in CRC is controversial. We evaluated survivin expression in formalin-fixed paraffin-embedded tumor samples of 188 patients with CRC by immunohistochemistry. Survivin over-expression was detected in 85 patients (45.2%) and was significantly associated with primary tumor sites (p=0.028), lymph node metastasis (p=0.029) and advanced III/IV CRC stages (AJCC 7; p=0.001). Furthermore, survivin up-regulation correlated with reduced disease-free survival (DFS; p=0.021) and overall survival (OS; p<0.000) and was proved to be an independent prognostic factor for both DFS and OS in multivariate analysis. Conclusion: Our data suggest that CD133+ CRC stem cells have a distinct expression pattern and that survivin, up-regulated by differentially expressed IL-4, is a candidate biomarker for the prediction of recurrence and survival in CRC.
AB - Background/Aim: CD133 is an important, but not exclusive, biomarker of colorectal cancer (CRC) stem cells. Materials and Methods: In order to identify other CRC stem cell-specific genes, we performed a comparative expression profiling of CD133+ and CD133- cell populations in primary and metastatic tumors from four patients with CRC. CD133+ and CD133- CRC cells were isolated using MagSweeper and used for whole-transcriptome analysis with RNA-Seq. Results: We found that in CD133+ cells, 17 genes (RNASE2, PRB2, IL4, MGC27382, CLEC4C, SALL3, GIMAP1, ISG15, LOC728875, ZIK1, ICAM2, CCDC7, CDYL2, LRRC2, ZEB1, OSTF1 and CCDC144B) were significantly up-regulated compared to CD133- CRC cells. Among them, IL4 has been known as an inducer of survivin implicated in the survival and proliferation of cancer cells. However, the prognostic value of survivin in CRC is controversial. We evaluated survivin expression in formalin-fixed paraffin-embedded tumor samples of 188 patients with CRC by immunohistochemistry. Survivin over-expression was detected in 85 patients (45.2%) and was significantly associated with primary tumor sites (p=0.028), lymph node metastasis (p=0.029) and advanced III/IV CRC stages (AJCC 7; p=0.001). Furthermore, survivin up-regulation correlated with reduced disease-free survival (DFS; p=0.021) and overall survival (OS; p<0.000) and was proved to be an independent prognostic factor for both DFS and OS in multivariate analysis. Conclusion: Our data suggest that CD133+ CRC stem cells have a distinct expression pattern and that survivin, up-regulated by differentially expressed IL-4, is a candidate biomarker for the prediction of recurrence and survival in CRC.
KW - Cancer stem cells
KW - CD133
KW - Interleukin-4
KW - Surviving
UR - https://www.scopus.com/pages/publications/84908145670
M3 - Article
C2 - 25331798
AN - SCOPUS:84908145670
SN - 1109-6535
VL - 11
SP - 259
EP - 266
JO - Cancer Genomics and Proteomics
JF - Cancer Genomics and Proteomics
IS - 5
ER -
