RRC ID 54814
Author Inoue K, Hatano K, Hanamatsu Y, Saigo C, Kito Y, Bunai K, Shibata T, Takeuchi T.
Title Pathobiological role of cleft palate transmembrane protein 1 family proteins in oral squamous cell carcinoma.
Journal J Cancer Res Clin Oncol
Abstract PURPOSE:Cleft palate transmembrane protein 1 (Clptm1) and its paralog protein, Cisplatin resistance-related protein 9 (CRR9) constitute a highly conserved protein family, from Caenorhabditis elegans to Homo sapiens. In the present study, we examined the clinicopathological and biological significance of Clptm1 and CRR9 expression in oral squamous cell carcinoma (OSCC).
METHODS:Ninety-eight OSCC tissue specimens were immunohistochemically stained with specific antibodies to Clptm1 and CRR9. The immunoreactivity of Clptm1 and CRR9 was then correlated with clinicopathological factors, including the prognosis of patients. siRNA-mediated gene silencing of CRR9 followed by cell proliferation, Matrigel invasion, anoikis assay, and gelatin zymography were performed using cultured OSCC cells. Subsequently, immunohistochemical examination including double staining was performed to determine the correlation between CRR9 and Bcl-xL expression in OSCC cells.
RESULTS:Non-tumorous oral squamous cells exhibited vague, weak, or little cytoplasmic staining with anti-Clptm1 and CRR9 antibodies. By contrast, robust Clptm1 and CRR9 immunoreactivity was found at the cancer invasion front in 55 and 54 of the 98 OSCC tissue specimens, respectively. Notably, CRR9 immunoreactivity was associated with more than 5 mm of depth of invasion, poor prognosis of the patients, and smoking habits (P < 0.05). siRNA-mediated gene silencing of CRR9 did not alter the cell proliferation but decreased Matrigel invasion and impaired anoikis resistance in cultured Ca9-22 and SAS cells. CRR9 and anti-apoptotic Bcl-xL expression levels were correlated in pT1 OSCC tissue specimens.
CONCLUSIONS:Clptm1 and CRR9 were overexpressed in many OSCC tissues. In particular, CRR9 expression may promote tumor development and have a significant poor prognostic value in OSCC, possibly through conferring invasion ability and resistance to apoptotic stimuli possibly related to Bcl-xL expression. CRR9 could be a novel molecular target for patients with OSCC.
Volume 145(4)
Pages 851-859
Published 2019-4
DOI 10.1007/s00432-019-02843-0
PII 10.1007/s00432-019-02843-0
PMID 30635792
MeSH Cell Line, Tumor Female Gene Silencing Humans Immunohistochemistry Male Membrane Proteins / biosynthesis* Membrane Proteins / genetics Middle Aged Mouth Neoplasms / genetics Mouth Neoplasms / metabolism* Mouth Neoplasms / pathology* Neoplasm Proteins / biosynthesis Neoplasm Proteins / genetics Neoplasm Staging Prognosis Retrospective Studies Squamous Cell Carcinoma of Head and Neck / genetics Squamous Cell Carcinoma of Head and Neck / metabolism* Squamous Cell Carcinoma of Head and Neck / pathology* bcl-X Protein / biosynthesis bcl-X Protein / genetics
IF 3.282
Times Cited 2
Resource
Human and Animal Cells SAS(RCB1974) Ca9-22(RCB1976)