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SMAD‑6, ‑7 and ‑9 are potential molecular biomarkers for the prognosis in human lung cancer
- Source :
- Oncology Letters
- Publication Year :
- 2020
- Publisher :
- Spandidos Publications, 2020.
-
Abstract
- SMADs, a family of proteins that function as signal transducers and transcriptional regulators to regulate various signaling pathways, including the transforming growth factor-β signaling pathway, are similar to the mothers against decapentaplegic family of genes and the sma gene family in Caenorhabditis elegans. SMADs generate context-dependent modulation by interacting with various sequence-specific transcription factors, such as E2F4/5, c-Fos, GATA3, YY1 and SRF, which have been found to serve a key role in lung carcinoma oncogenesis and progression. However, the prognostic values of the eight SMADs in lung cancer have not been fully understood. In the present study, the expression levels and survival data of SMADs in patients with lung carcinoma from the Oncomine, Gene Expression Profiling Interactive Analysis, Kaplan-Meier plotter and cBioPortal databases were downloaded and analyzed. It was found that the mRNA expression levels of SMAD-6, −7 and −9 were decreased in lung adenocarcinoma and squamous cell carcinoma compared with that in adjacent normal tissues, while there was no significant difference in SMADs 1–5. Survival analysis revealed that not only were low transcriptional levels of SMAD-6, −7 and −9 associated with low overall survival but they also had prognostic role for progression-free survival and post-progression survival (P
- Subjects :
- 0301 basic medicine
Cancer Research
Cancer
Articles
SMAD
Biology
medicine.disease
medicine.disease_cause
Gene expression profiling
lung cancer
03 medical and health sciences
030104 developmental biology
0302 clinical medicine
Oncology
030220 oncology & carcinogenesis
medicine
Cancer research
Carcinoma
biomarker
Adenocarcinoma
prognosis
Mothers against decapentaplegic
Lung cancer
Carcinogenesis
Subjects
Details
- ISSN :
- 17921082 and 17921074
- Volume :
- 20
- Database :
- OpenAIRE
- Journal :
- Oncology Letters
- Accession number :
- edsair.doi.dedup.....a2915472b34a20aa8a285dc16908b9f7
- Full Text :
- https://doi.org/10.3892/ol.2020.11851