Evidence map›Paper›PMID 38252332›Full record

ArticleMolecular biology reports2024

High prevalence of CD44 and its ligand low molecular weight hyaluronan in plasma of HNSCC patients: clinical significance.

Rituparna Roy, Nilanjana Chatterjee, Md Sadi Khan, Farhin Sultana, Arindam Roy, Sukanya Naskar, Rajdeep Guha, Sagar Sen, Jayanta Chakrabarti, Bishnu Pada Chatterjee and 2 more

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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12 authors at 1 institution in 1 country.

Rituparna RoyDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Nilanjana ChatterjeeDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Md Sadi KhanDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Farhin SultanaDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Arindam RoyDepartment of Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Sukanya NaskarDepartment of Head and Neck Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Rajdeep GuhaDepartment of Head and Neck Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Sagar SenDepartment of Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Jayanta ChakrabartiDepartment of Surgical Oncology, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Bishnu Pada ChatterjeeDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India.
Chinmay Kumar PandaDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India. ckpanda.cnci@gmail.com.ORCID http://orcid.org/0000-0002-0854-6978
Sankhadeep DuttaDepartment of Oncogene Regulation, Chittaranjan National Cancer Institute, Kolkata, West Bengal, India. eordeep@gmail.com.ORCID http://orcid.org/0000-0002-8144-4345
Chittaranjan National Cancer Institute · IN

Funding

Centre International de Recherche sur le Cancer CRA/ETR/2019/1Chittaranjan National Cancer Institute Institutional JRF FellowshipCSIR-JRF/NET grant 09/030(0083)/2019-EMR-IIndian Council of Medical Research 5/13/25/2019/NCD-IIIIndian Council of Medical Research Extramural GrantNational Academy of Sciences, india NASI Senior Scientist Platinum Jubilee Fellowship
6 · The paper itself

Abstract

backgroundThis study aims to evaluate the role of cancer stem cell marker, CD44, and its ligand HA as potential molecular biomarker for early detection of HNSCC. METHODS AND

resultsThe expression profile (mRNA/Protein) of CD44 variants were analysed in primary HNSCC lesions and plasma of the patients. Then, prevalence of HA variants was analysed in plasma of the patients. The mRNA expression of CD44 variants, CD44S and CD44v3, were significantly high in both early (stage I/II) and late (stage III/IV) invasive lesions, with predominant expression of CD44v3 in the late-stage lesions. In plasma of HNSCC patients, increased levels of SolCD44, CD44-ICD and unique 62 KD CD44 variants with respect to standard CD44S were seen, in comparison to their prevalence in plasma of normal individuals. The abundance of CD44-ICD and 62 KD variants were significantly high in plasma of late stage HNSCC patients. Interestingly, significantly high level of low molecular weight HA(LMW HA) with respect to high molecular weight HA(HMW HA) was seen in plasma of HNSCC patients irrespective of clinical stages. On the contrary, high HMW HA level in plasma of normal individuals was seen. The high level of LMW HA in plasma of HNSCC patients might be due to combinatorial effect of increased mRNA expression of HA synthesizing enzyme HAS1/2/3 and HA degrading enzyme HYAL1/2, as seen in the primary HNSCC samples.

conclusionThus, our data revealed the importance of specific CD44 and HA variants in plasma of HNSCC patients during its development as potential non-invasive molecular biomarker of the disease.

Indexed as

Head and Neck NeoplasmsHyaluronic AcidBiomarkersClinical RelevanceHumansHyaluronan ReceptorsLigandsMolecular WeightPrevalenceRNA, MessengerSquamous Cell Carcinoma of Head and NeckBiomarkersCD44 protein, humanHyaluronan ReceptorsHyaluronic AcidLigandsRNA, MessengerCD44-ICDCD44 variantHASHNSCC biomarkerHYALSolCD44

Identifiers

PMID38252332
OpenAlexW4391109497

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.