Evidence map›Paper›PMID 32902730›Full record

ArticleMedical oncology (Northwood, London, England)2020

MYH9 suppresses melanoma tumorigenesis, metastasis and regulates tumor microenvironment.

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

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2020. 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
1.4field-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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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  4. Non-Muscle Myosin II A: Friend or Foe in Cancer?International journal of molecular sciences · 2024
    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

6 authors at 2 institutions in 1 country.

Satyendra Kumar SinghLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India.
Sunita SinhaLaboratory of Vascular Immunology, Institute of Life Sciences, Bhubaneswar, 751023, India.
Jyotirmayee PadhanLaboratory 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 http://orcid.org/0000-0003-4539-8916
Institute of Life Sciences · INManipal Academy of Higher Education · IN

Funding

Department of Biotechnology , Ministry of Science and Technology 102/IFD/SAN/2237Department of Biotechnology , Ministry of Science and Technology BT/PR13045/BRB/10/1461/2015Department of Science and Technology, Ministry of Science and Technology EMR/2016/003932Science and Engineering Research Board PDF/2017/001017
6 · The paper itself

Abstract

Non-muscle myosin IIA heavy chain (MYH9) has been implicated in many physiological and pathological functions including cell adhesion, polarity, motility to cancer. However, its role in melanoma remains unexplored. The aim of our study was to evaluate the role of MYH9 in melanoma tumor development and metastasis and further to find out the potential underlying mechanisms. In this study, we evaluated the in vitro migratory and invasive properties and in vivo tumor development and metastasis in C57BL/6 mice by silencing MYH9 in B16F10 melanoma cells. Knocking down MYH9 enhanced migration and invasiveness of B16F10 cells in vitro. Furthermore, MYH9 silencing accelerated tumor growth and metastasis in melanoma subcutaneous and intravenous mouse models. Next, oncogenes analysis revealed epithelial-mesenchymal transition and Erk signaling pathway are being regulated with MYH9 expression. Finally, MYH9 silencing in B16F10 cells modulates the tumor microenvironment by manipulating the leukocytes and macrophages infiltration in tumors. These findings established the opposing role of MYH9 as a tumor suppressor in melanoma suggesting specific MYH9 based approaches in therapeutics.

Indexed as

AnimalsCarcinogenesisCell ProliferationEpithelial-Mesenchymal TransitionMelanoma, ExperimentalMiceMice, Inbred C57BLMyosin Heavy ChainsNeoplasm InvasivenessTumor MicroenvironmentMyh9 protein, mouseMyosin Heavy ChainsMelanomaMYH9TumorigenesisTumor microenvironment

Identifiers

PMID32902730
OpenAlexW3083924041

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.