Evidence map›Paper›PMID 33604392›Full record

ArticleJournal of immunology research2021

p75NTR/proBDNF Modulates Basal Cell Carcinoma (BCC) Immune Microenvironment via Necroptosis Signaling Pathway.

Qingli Lu, Yuanyuan Qu, Yuan Ding, Xiaojing Kang

Abstract read
In one paragraph

Article in Journal of immunology research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
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  4. The Role of the Neurotrophin Network in Skin Squamous Cell Cancer and the Novel Use of the Zebrafish System.JID innovations : skin science from molecules to population health · 2024
    Review
  5. Article
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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

4 authors.

Qingli LuDepartment of Dermatology and Venereology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830000, China.ORCID https://orcid.org/0000-0002-1185-0057
Yuanyuan QuDepartment of Dermatology and Venereology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830000, China.ORCID https://orcid.org/0000-0002-4861-2052
Yuan DingDepartment of Dermatology and Venereology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830000, China.ORCID https://orcid.org/0000-0002-9165-7467
Xiaojing KangDepartment of Dermatology and Venereology, People's Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830000, China.ORCID https://orcid.org/0000-0002-6325-7300

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Basal cell carcinoma (BCC) is the most common skin cancer. While most of the basal cell carcinomas were localized lesion and can be easily managed, the treatment options to the advanced basal cell carcinomas are still remarkably limited. In recent years, proBDNF and its receptor p75NTR have been reported to play important roles in various diseases, including cancers and psychotic disorders. However, the role of p75NTR/proBDNF signaling in basal cell carcinoma remains unclear. Here, we found that the expression level of p75NTR/proBDNF was decreased in basal cell carcinoma patient samples and cell lines. In vitro study showed overexpression of p75NTR/proBDNF could significantly facilitate tumor cell death, including inflammatory-silent apoptosis and lytic inflammatory activated necroptosis. In vivo study showed overexpression of p75NTR/proBDNF dramatically promotes tumor-associated macrophage (M1) and T cell recruitment in a syngeneic mouse model of BCC. These results show a crucial role for p75NTR/proBDNF signaling in basal cell carcinoma immune microenvironment.

Indexed as

Signal TransductionAnimalsBasal Cell CarcinomaCell LineCell ProliferationGene ExpressionHumansImmunohistochemistryMiceNecroptosisNerve Tissue ProteinsReceptor-Interacting Protein Serine-Threonine KinasesReceptors, Nerve Growth FactorTumor-Associated MacrophagesTumor MicroenvironmentNerve Tissue ProteinsNGFR protein, humanReceptor-Interacting Protein Serine-Threonine KinasesReceptors, Nerve Growth FactorRIPK1 protein, humanRIPK3 protein, human

Identifiers

PMID33604392
PMCPMC7870300

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Registered trials

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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.