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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

Updated: May 24, 2025

Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics
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Molecular Markers of Occult Lymph Node Metastasis in Head and Neck Squamous Cell Carcinoma (HNSCC) Patients.

Piero Giuseppe Meliante1, Sofia Pizzolante1, Luca Perna2

  • 1Department of Neuroscience, Mental Health and Sensory Organs (NESMOS), "Sapienza" University of Rome, Sant'Andrea Hospital, 00189 Rome, Italy.

Frontiers in Bioscience (Landmark Edition)
|February 28, 2025
PubMed
Summary

Accurate diagnosis of lymph node metastasis in head and neck cancer is challenging. This review identifies molecular markers like miR-205 and E-cadherin to improve detection and treatment for head and neck squamous cell carcinoma (HNSCC).

Keywords:
cancer markerhead and neck squamous cell carcinomalymp nodemeastasisoccult metastasisregional metastasis

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Area of Science:

  • Oncology
  • Molecular Biology
  • Pathology

Background:

  • Accurate diagnosis of regional lymph node metastasis is crucial for head and neck cancer (HNSCC) treatment planning.
  • Current radiological techniques face challenges in detecting nodal metastasis, potentially leading to undertreatment or overtreatment.
  • Identifying reliable molecular markers is essential to improve diagnostic accuracy in HNSCC.

Purpose of the Study:

  • To review and identify molecular markers associated with occult metastasis in head and neck squamous cell carcinoma (HNSCC).
  • To analyze markers based on their location: lymph node, tumor tissue, and blood.
  • To highlight promising markers for improved diagnostic precision in HNSCC.

Main Methods:

  • Comprehensive literature review of studies analyzing molecular markers in HNSCC.
  • Categorization of identified markers by analysis type: lymph node, tumor tissue, and blood.
  • Evaluation of marker effectiveness across various studies and subsites.

Main Results:

  • Numerous molecular markers were identified across lymph node, tumor tissue, and blood analyses.
  • Promising markers demonstrating effectiveness include miR-205, desmoglein 3 (DSG3), pan-cytokeratin (CK) AE1/AE3, HPV-16, activin-A, cyclin D1, E-cadherin, and neural progenitor lineage (NPL).
  • These markers show potential for enhancing the detection of occult metastasis in HNSCC.

Conclusions:

  • Several molecular markers show promise for improving the diagnosis of lymph node metastasis in HNSCC.
  • Combination scoring systems using these markers could enhance diagnostic precision.
  • Further research focusing on integrated marker approaches is recommended to optimize treatment selection for HNSCC patients.