Bibliographic Details
Title: |
Effects of somatic alterations at pathway level are more mechanism‐explanatory and clinically applicable to quantity of liver metastases of colorectal cancer |
Authors: |
Zhong‐guo Zhang, Fei Ma, Shuang Zhao, Xiaoyu Yang, Fang Liu, Chenghai Xue, Liren Liu, Jin Gu, Haozhe Piao |
Source: |
Cancer Medicine, Vol 8, Iss 10, Pp 4732-4742 (2019) |
Publisher Information: |
Wiley, 2019. |
Publication Year: |
2019 |
Collection: |
LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens |
Subject Terms: |
algorithm, cancer pathways, liver metastases lesions, somatic alterations, survival, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282 |
More Details: |
Abstract Background The quantity of metastases lesions is an important reference when it comes to making a more informed treatment decision for patients with colorectal cancer liver metastases. However, the molecular alterations in patients with different numbers of lesions have not been systematically studied. Methods We investigated somatic alterations and microsatellite instability (MSI) of liver metastases from patients with single, multiple or diffuse metastasis lesions. A new algorithm “Pathway Damage Score” was developed to comprehensively assess the functional impact of somatic alterations at the pathway level. Pathogenic pathways of different metastasis were identified and their prognosis effects were evaluated. Furthermore, the subnetworks and affected phenotypes of the altered genes in each pathogenic pathway were analyzed. Results Somatic alterations and altered genes occurred sporadically as well as in MSI state in different metastasis types, although MSS patients had more metastatic lesions than that of the MSI patients. Every metastasis group has their own pathogenic pathways and damaged “Cargo recognition for clathrin‐mediated endocytosis” is significantly associated with poor prognosis (P |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
2045-7634 |
Relation: |
https://doaj.org/toc/2045-7634 |
DOI: |
10.1002/cam4.2368 |
Access URL: |
https://doaj.org/article/b33be7c69f554cc291104e8c2d841b75 |
Accession Number: |
edsdoj.b33be7c69f554cc291104e8c2d841b75 |
Database: |
Directory of Open Access Journals |