Evidence map›Paper›PMID 30635792›Full record

ArticleJournal of cancer research and clinical oncology2019

Pathobiological role of cleft palate transmembrane protein 1 family proteins in oral squamous cell carcinoma.

Keisuke Inoue, Kiichi Hatano, Yuki Hanamatsu, Chiemi Saigo, Yusuke Kito, Katsuaki Bunai, Toshiyuki Shibata, Tamotsu Takeuchi

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  7. Clptm1, a new target in suppressing epileptic seizure by regulating GABAThe Kaohsiung journal of medical sciences · 2023
    Article
  8. Article
  9. Human colorectal cancer-associated carbohydrate antigen on annexin A2 protein.Journal of molecular medicine (Berlin, Germany) · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Keisuke InoueDepartment of Oral and Maxillofacial Surgery, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Kiichi HatanoDepartment of Oral and Maxillofacial Surgery, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Yuki HanamatsuDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Chiemi SaigoDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Yusuke KitoDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Katsuaki BunaiDepartment of Oral and Maxillofacial Surgery, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Toshiyuki ShibataDepartment of Oral and Maxillofacial Surgery, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan.
Tamotsu TakeuchiDepartment of Pathology and Translational Research, Gifu University Graduate School of Medicine, Yanagido, Gifu, 501-1193, Japan. takeutit08@gmail.com.ORCID http://orcid.org/0000-0002-4264-3632
Gifu University · JP

Funding

KAKEN 15K08361KAKEN 15K19051KAKEN 17K15642
6 · The paper itself

Abstract

purposeCleft 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).

methodsNinety-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.

resultsNon-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.

conclusionsClptm1 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.

Indexed as

bcl-X ProteinCell Line, TumorFemaleGene SilencingHumansImmunohistochemistryMaleMembrane ProteinsMiddle AgedMouth NeoplasmsNeoplasm ProteinsNeoplasm StagingPrognosisRetrospective StudiesSquamous Cell Carcinoma of Head and NeckBCL2L1 protein, humanbcl-X ProteinCLPTM1L protein, humanCLPTM1 protein, humanMembrane ProteinsNeoplasm ProteinsAnoikisClptm1CRR9Oral squamous cell carcinomaOutcome

Identifiers

PMID30635792
PMCPMC11810150
OpenAlexW2908681510

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.