Lai Xu 1 , Joseph Ziegelbauer 2 , Rong Wang 1 , Wells W Wu 3 , Rong-Fong Shen 3 , Hartmut Juhl 4 , Yaqin Zhang 1 , Amy Rosenberg 5 . Show Affiliations »
Abstract
PURPOSE: To gain insight into factors involved in tumor progression and metastasis, we examined the role of noncoding RNAs in the biologic characteristics of colorectal carcinoma, in paired samples of tumor together with normal mucosa from the same colorectal carcinoma patient. The tumor and healthy tissue samples were collected and stored under stringent conditions, thereby minimizing warm ischemic time. EXPERIMENTAL DESIGN: We focused particularly on distinctions among high-stage tumors and tumors with known metastases, performing RNA-Seq analysis that quantifies transcript abundance and identifies novel transcripts. RESULTS: In comparing 35 colorectal carcinomas, including 9 metastatic tumors (metastases to lymph nodes and lymphatic vessels), with their matched healthy control mucosa, we found a distinct signature of mitochondrial transfer RNAs (MT-tRNA) and small nucleolar RNAs (snoRNA) for metastatic and high-stage colorectal carcinoma. We also found the following: (i) MT-TF (phenylalanine) and snord12B expression correlated with a substantial number of miRNAs and mRNAs in 14 colorectal carcinomas examined; (ii) an miRNA signature of oxidative stress, hypoxia, and a shift to glycolytic metabolism in 14 colorectal carcinomas, regardless of grade and stage; and (iii) heterogeneous MT-tRNA/snoRNA fingerprints for 35 pairs. CONCLUSIONS: These findings could potentially assist in more accurate and predictive staging of colorectal carcinoma, including identification of those colorectal carcinomas likely to metastasize. ©2015 American Association for Cancer Research.
PURPOSE: To gain insight into factors involved in tumor progression and metastasis, we examined the role of noncoding RNAs in the biologic characteristics of colorectal carcinoma , in paired samples of tumor together with normal mucosa from the same colorectal carcinoma patient . The tumor and healthy tissue samples were collected and stored under stringent conditions, thereby minimizing warm ischemic time. EXPERIMENTAL DESIGN: We focused particularly on distinctions among high-stage tumors and tumors with known metastases , performing RNA-Seq analysis that quantifies transcript abundance and identifies novel transcripts. RESULTS: In comparing 35 colorectal carcinomas , including 9 metastatic tumors (metastases to lymph nodes and lymphatic vessels), with their matched healthy control mucosa, we found a distinct signature of mitochondrial transfer RNAs (MT-tRNA) and small nucleolar RNAs (snoRNA ) for metastatic and high-stage colorectal carcinoma . We also found the following: (i) MT-TF (phenylalanine ) and snord12B expression correlated with a substantial number of miRNAs and mRNAs in 14 colorectal carcinomas examined; (ii) an miRNA signature of oxidative stress, hypoxia , and a shift to glycolytic metabolism in 14 colorectal carcinomas , regardless of grade and stage; and (iii) heterogeneous MT-tRNA/snoRNA fingerprints for 35 pairs. CONCLUSIONS: These findings could potentially assist in more accurate and predictive staging of colorectal carcinoma , including identification of those colorectal carcinomas likely to metastasize. ©2015 American Association for Cancer Research.
Entities: CellLine
Chemical
Disease
Gene
Species
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Year: 2015
PMID: 26384739 PMCID: PMC4738054 DOI: 10.1158/1078-0432.CCR-15-0737
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531