Evidence map›Paper›PMID 32735377›Full record

ArticleJournal of cellular and molecular medicine2020

P2X7R promotes angiogenesis and tumour-associated macrophage recruitment by regulating the NF-κB signalling pathway in colorectal cancer cells.

Chunhui Yang, Shuang Shi, Ying Su, Jing-Shan Tong, Liangjun Li

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

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  10. The Significance of Aldehyde Dehydrogenase 1 in Cancers.International journal of molecular sciences · 2024
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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 2 countries.

Chunhui YangDepartment of Clinical Laboratory, the Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Shuang ShiDepartment of Clinical Laboratory, the Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Ying SuDepartment of Clinical Laboratory, the Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Jing-Shan TongDepartment of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID 0000-0001-7543-6341
Liangjun LiDepartment of Clinical Laboratory, the Second Affiliated Hospital of Dalian Medical University, Dalian, China.ORCID 0000-0001-8244-9597
Dalian Medical University · CNUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of P2X7R has been observed in several tumours and is related to cancer advancement and metastasis. However, the role of P2X7R in colorectal cancer (CRC) patients is not well understood. In the current study, overexpression of P2X7R and the effects at the molecular and functional levels in CRC were assessed in a mouse orthotopic model. Functional assays, such as the CCK-8 assay, wound healing and transwell assay, were used to determine the biological role of P2X7R in CRC cells. CSC-related genes and properties were detected via sphere formation and real-time PCR assays. The underlying mechanisms were explored by Western blotting, real-time PCR and Flow cytometry. In this study, we found that overexpression of P2X7R increases in the in vivo growth of tumours. P2X7R overexpression also increased CD31, VEGF and concurrent angiogenesis. P2X7R up-regulates aldehyde dehydrogenase-1 (ALDH1) and CSC characteristics. Transplanted tumour cells with P2X7R overexpression stimulated cytokines to recruit tumour-associated macrophage (TAMs) to increase the growth of tumours. We also found that the NF-κB signalling pathway is involved in P2X7R-induced cytokine up-regulation. P2X7R promotes NF-κB-dependent cytokine induction, which leads to TAM recruitment to control tumour growth and advancement and remodelling of the stroma. Our findings demonstrate that P2X7R plays a key role in TAM recruitment, which may be a therapeutic target for CRC patients.

Indexed as

AdenocarcinomaAnimalsCell Line, TumorCell MovementColorectal NeoplasmsCytokinesGene Knockdown TechniquesHumansMiceMice, Inbred BALB CNeoplasm InvasivenessNeoplasm ProteinsNeovascularization, PathologicNF-kappa BReceptors, Purinergic P2X7Recombinant ProteinsCytokinesNeoplasm ProteinsNF-kappa BP2RX7 protein, humanP2rx7 protein, mouseReceptors, Purinergic P2X7Recombinant Proteinsangiogenesiscancer stem cellsNF-κBP2X7RTAMstumour growth

Identifiers

PMID32735377
PMCPMC7521273
OpenAlexW3046392777

What OpenQuestion holds

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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.