Evidence map›Paper›PMID 38679985›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

Expression of CLLD7 and CHC1L Proteins in Oral Epithelial Dysplasia in a Group of Thai Patients.

Patcharanun Wiphakphongpakorn, Rachai Juengsomjit, Sopee Poomsawat, Ounruean Meesakul, Bishwa Prakash Bhattarai, Boworn Klongnoi, Waranun Buajeeb, Siribang-On Piboonniyom Khovidhunkit

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Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Patcharanun WiphakphongpakornDepartment of Oral Medicine and Periodontology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Rachai JuengsomjitDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Sopee PoomsawatDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Ounruean MeesakulDepartment of Oral and Maxillofacial Pathology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Bishwa Prakash BhattaraiInstitute of Oral Biology, Faculty of Dentistry, University of Oslo, Oslo, Norway.
Boworn KlongnoiDepartment of Oral and Maxillofacial Surgery, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Waranun BuajeebDepartment of Oral Medicine and Periodontology, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
Siribang-On Piboonniyom KhovidhunkitDepartment of Advanced General Dentistry, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.ORCID 0000-0002-4496-7964

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPrevious study showed aberrant CLLD7 and CHC1L protein expression in oral squamous cell carcinoma (OSCC) compared to normal oral mucosa (NOM). This study aimed to evaluate the expression of these proteins in oral epithelial dysplasia (OED). MATERIALS AND

methodsForty specimens of OED and 11 NOM were used. The expression of CLLD7 and CHC1L was determined by immunohistochemistry. In each case, at least 1000 cells were counted. Presence of nuclear, cytoplasmic, and/or membrane staining of CLLD7 and CHC1L were considered positive. Percentages of total positive cells and positive cells at different locations were recorded. SPSS version 18 was used to compare variation between groups with statistical significance at p<0.05.

resultsNo significant differences in the percentages of total positive cells of CLLD7 and CHC1L were found between NOM and all grades of OED. Nevertheless, there were significant differences in subcellular staining of these two proteins. In CLLD7, the nuclear staining of the moderate and the severe OED groups was significantly lower than that of the NOM group (p<0.05). The percentages of membrane staining of CHC1L in moderate and severe OED were significantly higher than that of NOM (p<0.001). In addition, the nuclear staining of CHC1L in each grade of OED was significantly lower than that of NOM (p<0.05).

conclusionThe subcellular mislocalization of CLLD7 and CHC1L in OED suggests that the expression of these potential tumor suppressor proteins might be dysregulated during the dysplastic process. The distinct membrane staining of CHC1L observed in OED but not in NOM is a useful characteristic that can be used to separate OED from NOM. Thus, CHC1L may be a good marker to assist in the diagnosis of OED.

Indexed as

Biomarkers, TumorCarcinoma, Squamous CellMouth MucosaMouth NeoplasmsSoutheast Asian PeopleAdultAgedCase-Control StudiesFemaleFollow-Up StudiesGuanine Nucleotide Exchange FactorsHumansMaleMiddle AgedNeoplasm ProteinsPrecancerous ConditionsBiomarkers, TumorGuanine Nucleotide Exchange FactorsNeoplasm ProteinsRCBTB1 protein, humanRCBTB2 protein, humancancerCHC1LCLLD7normal oral mucosaoral epithelial dysplasia

Identifiers

PMID38679985
PMCPMC11162717

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