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Preliminary Study on the Expression of CLLD7 and CHC1L Proteins in Oral Squamous Cell Carcinoma

Overview
Journal Eur J Dent
Publisher Thieme
Specialty Dentistry
Date 2023 Jun 13
PMID 37311552
Authors
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Abstract

Objective:  This study aimed to preliminarily evaluate the expression of two putative tumor suppressor proteins, including chronic lymphocytic leukemia deletion gene 7 (CLLD7) and chromosome condensation 1-like (CHC1L) proteins in oral squamous cell carcinoma (OSCC).

Materials And Methods:  Expression of CLLD7 and CHC1L proteins was analyzed in 19 OSCC and 12 normal oral mucosa (NOM) using immunohistochemistry. The percentage of positive cells and intensity of staining were semiquantitatively assessed and expressed with an immunoreactive score. The number of positive cells at various subcellular localizations was evaluated and presented in percentages. The immunoreactivity scores and percentages of positive cells at various localizations were compared between the normal and OSCC groups with statistical significance at -value less than 0.05.

Results:  According to immunohistochemical analysis, the immunoreactivity scores for both CLLD7 and CHC1L were higher in NOM than those of OSCC. Analysis of CLLD7 localization revealed predominant nuclear staining at basal and parabasal areas in NOM, whereas more cytoplasmic staining was observed in OSCC. For CHC1L, nuclear staining was prominent in NOM. In contrast, significantly increased plasma membrane staining was detected in OSCC.

Conclusion:  The expression of CLLD7 and CHC1L proteins was reduced in OSCC. Alterations in the subcellular localization of these two proteins in OSCC were also demonstrated. These preliminary results suggest that CLLD7 and CHC1L are aberrantly expressed in OSCC. The precise mechanisms of these putative tumor suppressor proteins in OSCC require future studies.

Citing Articles

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

Wiphakphongpakorn P, Juengsomjit R, Poomsawat S, Meesakul O, Bhattarai B, Klongnoi B Asian Pac J Cancer Prev. 2024; 25(4):1257-1264.

PMID: 38679985 PMC: 11162717. DOI: 10.31557/APJCP.2024.25.4.1257.

References
1.
Latil A, Morant P, Fournier G, Mangin P, Berthon P, Cussenot O . CHC1-L, a candidate gene for prostate carcinogenesis at 13q14.2, is frequently affected by loss of heterozygosity and underexpressed in human prostate cancer. Int J Cancer. 2002; 99(5):689-96. DOI: 10.1002/ijc.10393. View

2.
Dodson M, Cliby W, Xu H, DeLacey K, Hu S, Keeney G . Evidence of functional RB protein in epithelial ovarian carcinomas despite loss of heterozygosity at the RB locus. Cancer Res. 1994; 54(3):610-3. View

3.
Hadjebi O, Casas-Terradellas E, Garcia-Gonzalo F, Rosa J . The RCC1 superfamily: from genes, to function, to disease. Biochim Biophys Acta. 2008; 1783(8):1467-79. DOI: 10.1016/j.bbamcr.2008.03.015. View

4.
Wang X, Li S . Protein mislocalization: mechanisms, functions and clinical applications in cancer. Biochim Biophys Acta. 2014; 1846(1):13-25. PMC: 4141035. DOI: 10.1016/j.bbcan.2014.03.006. View

5.
Kaemmerer D, Peter L, Lupp A, Schulz S, Sanger J, Baum R . Comparing of IRS and Her2 as immunohistochemical scoring schemes in gastroenteropancreatic neuroendocrine tumors. Int J Clin Exp Pathol. 2012; 5(3):187-94. PMC: 3341681. View