Evidence map›Paper›PMID 33052434›Full record

ReviewCellular and molecular life sciences : CMLS2021

Low molecular weight protein tyrosine phosphatase as signaling hub of cancer hallmarks.

Alessandra V S Faria, Emanuella Maria Barreto Fonseca, Helon Guimarães Cordeiro, Stefano Piatto Clerici, Carmen Veríssima Ferreira-Halder

Open access · bronzeAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  4. Review
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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

5 authors at 3 institutions in 2 countries.

Alessandra V S FariaDepartment of Biochemistry and Tissue Biology, University of Campinas, Campinas, São Paulo, Brazil.
Emanuella Maria Barreto FonsecaDepartment of Biochemistry and Tissue Biology, University of Campinas, Campinas, São Paulo, Brazil.
Helon Guimarães CordeiroDepartment of Biochemistry and Tissue Biology, University of Campinas, Campinas, São Paulo, Brazil.
Stefano Piatto ClericiDepartment of Biochemistry and Tissue Biology, University of Campinas, Campinas, São Paulo, Brazil.
Carmen Veríssima Ferreira-HalderDepartment of Biochemistry and Tissue Biology, University of Campinas, Campinas, São Paulo, Brazil. carmenv@unicamp.br.
Universidade Estadual de Campinas (UNICAMP) · BRErasmus MC · NLUniversidade Federal de São Paulo · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 141723/2019-0Conselho Nacional de Desenvolvimento Científico e Tecnológico 303900/2017-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/11433-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/20412-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2017/08119-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/03593-6
6 · The paper itself

Abstract

In the past decade, significant progress has been made in understanding the role of protein tyrosine phosphatase as a positive regulator of tumor progression. In this scenario, our group was one of the first to report the involvement of the low molecular weight protein tyrosine phosphatase (LMWPTP or ACP1) in the process of resistance and migration of tumor cells. Later, we and others demonstrated a positive correlation between the amount of this enzyme in human tumors and the poor prognosis. With this information in mind, we asked if LMWPTP contribution to metastasis, would it have an action beyond the primary tumor site. We know that the amount of this enzyme in the tumor cell correlates positively with the ability of cancer cells to interact with platelets, an indication that this enzyme is also important for the survival of these cells in the bloodstream. Here, we discuss several molecular aspects that support the idea of LMWPTP as a signaling hub of cancer hallmarks. Chemical and genetic modulation of LMWPTP proved to shut down signaling pathways associated with cancer aggressiveness. Therefore, advances in the development of LMWPTP inhibitors have great applicability in human diseases such as cancer.

Indexed as

Biomarkers, TumorHumansMolecular WeightNeoplasmsPhosphorylationProtein Tyrosine PhosphatasesProto-Oncogene ProteinsSignal TransductionACP1 protein, humanBiomarkers, TumorProtein Tyrosine PhosphatasesProto-Oncogene ProteinsCancer hallmarksLow molecular weight protein tyrosine phosphataseMetabolism reprogrammingSignaling hub

Identifiers

PMID33052434
PMCPMC11073135
OpenAlexW3092424167

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.