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pmid:30700932

Identification of liver metastasis-associated genes in human colon carcinoma by mRNA profiling.

Jianling Liu · Dan Wang · Chaoqi Zhang · Zhen Zhang · Xinfeng Chen · Jingyao Lian · Jinbo Liu · Guixian Wang · Weitang Yuan · Zhenqiang Sun · Weijia Wang · Mengjia Song · Yaping Wang · Qian Wu · Ling Cao · Dong Wang · Yi Zhang

Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2018 doi:10.21147/j.issn.1000-9604.2018.06.08

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Identification of liver metastasis-associated genes in human colon carcinoma by mRNA profiling.
doi
10.21147/j.issn.1000-9604.2018.06.08
pmid
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Jianling Liu
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Dan Wang
[2]
Chaoqi Zhang
[3]
Zhen Zhang
[4]
Xinfeng Chen
[5]
Jingyao Lian
[6]
Jinbo Liu
[7]
Guixian Wang
[8]
Weitang Yuan
[9]
Zhenqiang Sun
[10]
Weijia Wang
[11]
Mengjia Song
[12]
Yaping Wang
[13]
Qian Wu
[14]
Ling Cao
[15]
Dong Wang
[16]
Yi Zhang
journal
Chinese journal of cancer research = Chung-kuo yen cheng yen chiu
year
2018
abstract
OBJECTIVE: Liver metastasis, which contributes substantially to high mortality, is the most common recurrent mode of colon carcinoma. Thus, it is necessary to identify genes implicated in metastatic colonization of the liver in colon carcinoma. METHODS: We compared mRNA profiling in 18 normal colon mucosa (N), 20 primary tumors (T) and 19 liver metastases (M) samples from the dataset GSE49355 and GSE62321 of Gene Expression Omnibus (GEO) database. Gene ontology (GO) and pathways of the identified genes were analyzed. Co-expression network and protein-protein interaction (PPI) network were employed to identify the interaction relationship. Survival analyses based on The Cancer Genome Atlas (TCGA) database were used to further screening. Then, the candidate genes were validated by our data. RESULTS: We identified 22 specific genes related to liver metastasis and they were strongly associated with cell migration, adhesion, proliferation and immune response. Simultaneously, the results showed that C-X-C motif chemokine ligand 14 (CXCL14) might be a favorable prediction factor for survival of patients with colon carcinoma. Importantly, our validated data further suggested that lower CXCL14 represented poorer outcome and contributed to metastasis. Gene set enrichment analysis (GSEA) showed that CXCL14 was negatively related to the regulation of stem cell proliferation and epithelial to mesenchymal transition (EMT). CONCLUSIONS: CXCL14 was identified as a crucial anti-metastasis regulator of colon carcinoma for the first time, and might provide novel therapeutic strategies for colon carcinoma patients to improve prognosis and prevent metastasis.
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