Evidence map›Paper›PMID 34711805›Full record

ArticleCell death & disease2021

p32 promotes melanoma progression and metastasis by targeting EMT markers, Akt/PKB pathway, and tumor microenvironment.

Sunita Sinha, Satyendra Kumar Singh, Nitish Jangde, Rashmi Ray, Vivek Rai

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  13. gC1qR: A New Target for Cancer Immunotherapy.Frontiers in immunology · 2023
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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 2 institutions in 1 country.

Sunita SinhaLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India.ORCID 0000-0001-6497-9420
Satyendra Kumar SinghLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India.
Nitish JangdeLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India.
Rashmi RayLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India.
Vivek RaiLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India. vivekrai.a@gmail.com.ORCID 0000-0003-4539-8916
Institute of Life Sciences · INManipal Academy of Higher Education · IN

Funding

Department of Biotechnology, Ministry of Science and Technology (DBT) 102/IFD/SAN/2237Department of Biotechnology, Ministry of Science and Technology (DBT) BT/PR13045/BRB/10/1461/2015
6 · The paper itself

Abstract

Melanoma originates from melanin-producing cells called melanocytes. Melanoma poses a great risk because of its rapid ability to spread and invade new organs. Cellular metastasis involves alteration in the gene expression profile and their transformation from epithelial to mesenchymal state. Despite of several advances, metastatic melanoma being a key cause of therapy failure and mortality remains poorly understood. p32 has been found to be involved in various physiological and pathophysiological conditions. However, the role of p32 in melanoma progression and metastasis remains underexplored. Here, we identify the role of p32 in the malignancy of both murine and human melanoma. p32 knockdown leads to reduced cell proliferation, migration, and invasion in murine and human melanoma cells. Furthermore, p32 promotes in vitro tumorigenesis, inducing oncogenes and EMT markers. Mechanistically, we show p32 regulates tumorigenic and metastatic properties through the Akt/PKB signaling pathway in both murine and human melanoma. Furthermore, p32 silencing attenuates melanoma tumor progression and lung metastasis in vivo, modulating the tumor microenvironment by inhibiting the angiogenesis, infiltration of macrophages, and leukocytes in mice. Taken together, our findings identify that p32 drives melanoma progression, metastasis, and regulates the tumor microenvironment. p32 can be a target of a novel therapeutic approach in the regulation of melanoma progression and metastasis.

Indexed as

AnimalsCarrier ProteinsCell MovementCell ProliferationDisease ProgressionEpithelial-Mesenchymal TransitionHumansMelanomaMiceMitochondrial ProteinsNeoplasm MetastasisProto-Oncogene Proteins c-aktSignal TransductionSurvival AnalysisTransfectionTumor MicroenvironmentC1QBP protein, humanCarrier ProteinsMitochondrial ProteinsProto-Oncogene Proteins c-akt

Identifiers

PMID34711805
PMCPMC8553772
OpenAlexW3208122506

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.