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1.
Sci Rep ; 9(1): 12913, 2019 09 09.
Article in English | MEDLINE | ID: mdl-31501464

ABSTRACT

The median overall survival (OS) of some head and neck malignancies, such as head and neck squamous cell carcinoma (HNSCC), with metastatic lesions was only 12 months. Whether aggressive pulmonary metastasectomy (PM) improves survival is controversial. Patients with primary head and neck malignancy undergoing PM were enrolled. Clinical outcomes were compared among different histological types. Whole-exome sequencing was used for matched pulmonary metastatic samples. The genes where genetic variants have been identified were sent for analysis by DAVID, IPA, and STRING. Forty-nine patients with primary head and neck malignancies were enrolled. Two-year postmetastasectomy survival (PMS) rates of adenoid cystic carcinoma, thyroid carcinoma, nasopharyngeal carcinoma, and HNSCC were 100%, 88.2%, 71.4%, and 59.2%, respectively (P = 0.024). In HNSCC, the time to distant metastasis was an independent predictive factor of the efficacy of PM. Several pathways, such as branched-chain amino acid (BCAA) consumption, were significantly associated with the progression of HNSCC [P < 0.001, fold enrichment (FE) = 5.45]. Moreover, metabolism-associated signaling pathways also seemed to be involved in cancer metastasis. Histological types and time to distant metastasis were important factors influencing the clinical outcomes of PM. For HNSCC, metabolic-associated signaling pathways were significantly associated with tumor progression and distant metastasis. Future validations are warranted.


Subject(s)
Genomics , Head and Neck Neoplasms/genetics , Head and Neck Neoplasms/pathology , Lung Neoplasms/secondary , Biomarkers, Tumor , Computational Biology/methods , Disease Progression , Disease Susceptibility , Female , Gene Ontology , Gene Regulatory Networks , Genomics/methods , Head and Neck Neoplasms/mortality , Humans , Lung Neoplasms/surgery , Male , Metastasectomy , Neoplasm Metastasis , Prognosis , Radiography, Thoracic , Tomography, X-Ray Computed , Exome Sequencing
3.
Sci Rep ; 8(1): 2713, 2018 02 09.
Article in English | MEDLINE | ID: mdl-29426835

ABSTRACT

Overexpression of ALDH is associated with cancer stem-like features and poor cancer prognosis. High ALDH activity has been observed in cancer stem-like cells. There are a total of 19 human ALDH isoforms, all of which are associated with reducing oxidative stress and protecting cells from damage. However, it is unknown whether all ALDHs are associated with poor cancer prognosis and which ones play a significant role in cancer progression. In this study, we used RNA sequencing data from The Cancer Genome Atlas (TCGA) to evaluate the differential expression of 19 ALDH isoforms in 5 common human cancers. The 19 ALDH genes were analyzed with an integrating meta-analysis of cancer prognosis. Genotyping and next-generation RNA sequencing for 30 pairwise samples of head and neck squamous cell carcinoma were performed and compared with the TCGA cohort. The analysis showed that each ALDH isoform had a specific differential expression pattern, most of which were related to prognosis in human cancer. A lower expression of ALDH2 in the tumor was observed, which was independent from the ALDH2 rs671 SNP variant and the expression of other mitochondria-associated protein coding genes. This study provides new insight into the association between ALDH expression and cancer prognosis.


Subject(s)
Aldehyde Dehydrogenase/genetics , Biomarkers, Tumor/genetics , Carcinoma, Squamous Cell/pathology , Gene Expression Profiling/methods , Gene Expression Regulation, Enzymologic , Head and Neck Neoplasms/pathology , Polymorphism, Single Nucleotide , Aldehyde Dehydrogenase/classification , Aldehyde Dehydrogenase/metabolism , Carcinoma, Squamous Cell/genetics , Carcinoma, Squamous Cell/metabolism , Case-Control Studies , Cell Movement , Cell Proliferation , Cohort Studies , Follow-Up Studies , Gene Expression Regulation, Neoplastic , Head and Neck Neoplasms/genetics , Head and Neck Neoplasms/metabolism , Humans , Isoenzymes , Prognosis , Survival Rate , Tumor Cells, Cultured
4.
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