Evidence map›Paper›PMID 32356317›Full record

ArticleJournal of cellular physiology2020

p120-catenin suppresses proliferation and tumor growth of oral squamous cell carcinoma via inhibiting nuclear phospholipase C-γ1 signaling.

Lusha Li, Shangli Ji, Chandrama Shrestha, Yi Jiang, Liyan Liao, Feng Xu, Zhenming Liu, Daniel D Bikle, Zhongjian Xie

Open access · greenAbstract read
In one paragraph

Article in Journal of cellular physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Functions of p120-catenin in physiology and diseases.Frontiers in molecular biosciences · 2024
    Review
  7. Article
  8. Overexpression of PTPRZ1 Regulates p120/Journal of oncology · 2022
    Article
  9. The basis of nuclear phospholipase C in cell proliferation.Advances in biological regulation · 2021
    Review
  10. Review
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

9 authors at 2 institutions in 2 countries.

Lusha LiNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, Institute of Metabolism and Endocrinology, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Shangli JiNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, Institute of Metabolism and Endocrinology, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Chandrama ShresthaNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, Institute of Metabolism and Endocrinology, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Yi JiangDepartment of Pathology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Liyan LiaoDepartment of Pathology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Feng XuNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, Institute of Metabolism and Endocrinology, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Zhenming LiuNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, Institute of Metabolism and Endocrinology, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.
Daniel D BikleEndocrine Unit, Veterans Affairs Medical Center, University of California San Francisco, San Francisco, California.
Zhongjian XieNational Clinical Research Center for Metabolic Diseases, Hunan Provincial Key Laboratory of Metabolic Bone Diseases, Institute of Metabolism and Endocrinology, and Department of Metabolism and Endocrinology, The Second Xiangya Hospital of Central South University, Changsha, Hunan, China.ORCID 0000-0002-1601-1156
Central South University · CNSan Francisco VA Medical Center · US

Funding

Vitamin D Receptor Coactivators in KeratinocytesR01AR050023 · NIAMS · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI BIKLE, DANIEL DAVID · 2004 to 2014
$3.4M
VITAMIN D AND THE DIFFERENTIATION OF KERATINOCYTESR01AR038386 · NIAMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI BIKLE, DANIEL DAVID · 1987 to 2003
$1.1M
Role of p120-catenin in oral squamous cell carcinomaR21DE019529 · NIDCR · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI XIE, ZHONGJIAN · 2009 to 2010
$424k
The role of PIKE-S in mediating EGFR mitogenic signaling in OSCC cellsR03DE018001 · NIDCR · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI XIE, ZHONGJIAN · 2007 to 2008
$157k
Role of vitamin D and calcium signaling in wound healingI01BX001066 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI BIKLE, DANIEL DAVID · 2011 to 2014
–
Vitamin D and Calcium signaling in epidermal stem cell maintenance, activation, and functionI01BX003814 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI BIKLE, DANIEL DAVID · 2018 to 2021
–
BLRD VA I01 BX001066BLRD VA I01 BX003814NIAMS NIH HHS R01 AR038386NIAMS NIH HHS R01 AR050023NIDCR NIH HHS R03 DE018001NIDCR NIH HHS R21 DE019529
6 · The paper itself

Abstract

p120-catenin (p120) serves as a stabilizer of the calcium-dependent cadherin-catenin complex and loss of p120 expression has been observed in several types of human cancers. The p120-dependent E-cadherin-β-catenin complex has been shown to mediate calcium-induced keratinocyte differentiation via inducing activation of plasma membrane phospholipase C-γ1 (PLC-γ1). On the other hand, PLC-γ1 has been shown to interact with phosphatidylinositol 3-kinase enhancer in the nucleus and plays a critical role in epidermal growth factor-induced proliferation of oral squamous cell carcinoma (OSCC) cells. To determine whether p120 suppresses OSCC proliferation and tumor growth via inhibiting PLC-γ1, we examined effects of p120 knockdown or p120 and PLC-γ1 double knockdown on proliferation of cultured OSCC cells and tumor growth in xenograft OSCC in mice. The results showed that knockdown of p120 reduced levels of PLC-γ1 in the plasma membrane and increased levels of PLC-γ1 and its signaling in the nucleus in OSCC cells and OSCC cell proliferation as well as xenograft OSCC tumor growth. However, double knockdown of p120 and PLC-γ1 or knockdown of PLC-γ1 alone did not have any effect. Immunohistochemical analysis of OSCC tissue from patients showed a lower expression level of p120 and a higher expression level of PLC-γ1 compared with that of adjacent noncancerous tissue. These data indicate that p120 suppresses OSCC cell proliferation and tumor growth by inhibiting signaling mediated by nuclear PLC-γ1.

Indexed as

Calcium, DietaryCarcinoma, Squamous CellCateninsCell DifferentiationCell ProliferationEpidermal Growth FactorHead and Neck NeoplasmsMouth NeoplasmsPhospholipase C gammaSignal TransductionSquamous Cell Carcinoma of Head and NeckCalcium, DietaryCateninsEpidermal Growth FactorPhospholipase C gammacell proliferation and differentiationp120-cateninphospholipase C-γ1squamous cell carcinoma cells (OSCC)

Identifiers

PMID32356317
PMCPMC7529923
OpenAlexW3022104257

What OpenQuestion holds

Textmetadata
LicenceTDM
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.