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GSE87211

GSE GEO
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Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery

Organism: Homo sapiens
Platform: GPL13497
Samples: 363
Experiment Types:
Expression profiling by array
Submitted: Sep 22 2016
Last Updated: Jan 09 2018
Status: Public on Nov 28 2017
Contact: Yue,,Hu (NCI)

Relations

BioProject: https://www.ncbi.nlm.nih.gov/bioproject/PRJNA343887

Summary

To understand the molecular mechanism of rectal cancer and develop markers for disease prognostication, we generated and explored a dataset from 243 rectal cancer patients by gene expression microarray analysis of cancer samples and matched controls, and SNP-arrays of germline DNA. We found that two of the loci most strongly linked with colorectal cancer (CRC) risk, 8q24 (upstream of MYC) and 18q21 (in the intron of SMAD7), as well as 20q13 (in the intron of LAMA5), are tightly associated with the prognosis of rectal cancer patients. For SNPs on 18q21 (rs12953717 and rs4464148) and 20q13 (rs4925386), alleles that correlate with higher risk for the development of CRC are associated with shorter disease free survival (DFS). However, for rs6983267 on 8q24, the low risk allele is associated with a higher risk for recurrence and metastasis after surgery, and importantly, is strongly correlated with the resistance of CRC cell lines to chemoradiotherapy (CRT). We also found that although MYC expression is dramatically increased in cancer, patients with higher levels of MYC have a better prognosis. The expression of SMAD7 is weakly correlated with DFS. Notably, the presence of the 8q24 and 18q21 SNP alleles is not correlated with expression levels of MYC and SMAD7. rs4464148, and probably rs6983267 and rs4925386, are linked with overall survival time of patients. In conclusion, we show that several CRC risk SNPs detect subpopulations of rectal cancer patients with poor prognosis, and that rs6983267 probably affects prognosis through interfering with the resistance of cancer cells to CRT.

Overall Design

Dataset of expression microarray of cancer samples and matched mucosa control, as well as SNP arrays of DNA extracted from peripheral blood lymphocytes from 230 rectal cancer patients was generated and analyzed together with patient's clinical data and long-term follow-up.

Analysis (1 step)

View Data Processing
Processing steps for GSE87211
  1. Raw data were log2 transformed and normalized to 75 percentile according to Agilent protocol.

Supplementary Files (1)

GSE87211_RAW.tar Download
GEO Samples (363)
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Dataset Citations (1)

Linked Publications (1)