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Related Concept Videos

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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Related Experiment Video

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Utilizing 18F-FDG PET/CT Imaging and Quantitative Histology to Measure Dynamic Changes in the Glucose Metabolism in Mouse Models of Lung Cancer
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Labyrinthin Expression Is Associated with Poor Prognosis in Patients with Non-Small-Cell Lung Cancer.

Weijie Ma1,2, Jie Zeng1, Dennis J Montoya3,4

  • 1Division of Hematology/Oncology, Department of Internal Medicine, University of California Davis School of Medicine, University of California Davis Comprehensive Cancer Center, Sacramento, CA 95817, USA.

Cancers
|February 11, 2023
PubMed
Summary

Labyrinthin (LAB) is highly expressed in most non-small-cell lung cancers (NSCLC). High LAB expression correlates with poorer survival and advanced disease, identifying it as a prognostic factor for NSCLC patients.

Keywords:
RNA sequencingTCGAlabyrinthinlung adenocarcinomalung squamous cell carcinomanon-small-cell lung cancerprognosistissue microarray

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Area of Science:

  • Oncology
  • Molecular Pathology

Background:

  • Non-small-cell lung cancer (NSCLC) remains a leading cause of cancer mortality worldwide.
  • Identifying novel prognostic biomarkers and therapeutic targets is crucial for improving patient outcomes.

Purpose of the Study:

  • To investigate the expression of Labyrinthin (LAB) in NSCLC.
  • To evaluate the association of LAB expression with clinical characteristics and patient survival.
  • To assess LAB as a potential biomarker for patient selection in clinical trials.

Main Methods:

  • Immunohistochemistry (IHC) on tissue microarrays from 256 NSCLC samples.
  • Propensity-score-weighted survival analyses (Kaplan-Meier and Cox models).
  • Analysis of LAB mRNA expression in The Cancer Genome Atlas (TCGA) datasets for lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC).

Main Results:

  • LAB protein expression was detected in 81.3% of NSCLC cases, present in both LUAD and LUSC.
  • Positive LAB IHC expression was significantly associated with poor overall survival (HR = 3.56) and higher tumor grade/metastasis.
  • LAB expression was confirmed as an independent prognostic factor for NSCLC.
  • LAB mRNA levels were elevated in primary and advanced LUAD tumors and correlated with poorer survival, but not significantly in LUSC.

Conclusions:

  • Labyrinthin is frequently expressed in NSCLC and serves as a significant independent prognostic biomarker.
  • LAB expression may guide patient stratification for targeted therapies, including the ongoing Phase I trial for LAB vaccines.