Evidence map›Paper›PMID 36848930›Full record

ArticleInternational journal of immunopathology and pharmacology

Immunopotentiation effects of apigenin on NK cell proliferation and killing pancreatic cancer cells.

Yong-Bo Feng, Ling Chen, Fu-Xing Chen, Yang Yang, Guo-Hua Chen, Zhong-Hai Zhou, Chun-Fang Xu

Open access · goldAbstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

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  17. Research Progress ofIntegrative cancer therapies
    Review
  18. Phytochemicals in Cancer Chemoprevention: Preclinical and Clinical Studies.Cancer control : journal of the Moffitt Cancer Center
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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

7 authors at 3 institutions in 1 country.

Yong-Bo FengDepartment of Gastroenterology, 74566The First Affiliated Hospital of Soochow University, Jiangsu, China.ORCID 0000-0003-2460-4696
Ling ChenDepartment of Central Laboratory, the 71st Group Army Hospital of PLA Army, The Affiliated Huaihai Hospital of Xuzhou Medical University, Jiangsu, China.
Fu-Xing ChenDepartment of Central Laboratory, the 71st Group Army Hospital of PLA Army, The Affiliated Huaihai Hospital of Xuzhou Medical University, Jiangsu, China.
Yang YangDepartment of Pharmacy, the 71st Group Army Hospital of PLA Army, The Affiliated Huaihai Hospital of Xuzhou Medical University, Jiangsu, China.ORCID 0000-0001-5618-3940
Guo-Hua ChenDepartment of General Surgery, Nanjing Gaochun Hospital of Chinese Medicine, Jiangsu, China.
Zhong-Hai ZhouDepartment of Central Laboratory, the 71st Group Army Hospital of PLA Army, The Affiliated Huaihai Hospital of Xuzhou Medical University, Jiangsu, China.ORCID 0000-0003-3683-7200
Chun-Fang XuDepartment of Gastroenterology, 74566The First Affiliated Hospital of Soochow University, Jiangsu, China.
Xuzhou Medical College · CNSoochow University · CNGaochun People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apigenin is a kind of flavonoid with many beneficial biological effects. It not only has direct cytotoxicity to tumor cells, but also can boost the antitumor effect of immune cells by modulating immune system. The purpose of this study was to investigate the proliferation of NK cells treated with apigenin and its cytotoxicity to pancreatic cancer cells in vitro, and explore its potential molecular mechanism. In this study, the effect of apigenin on NK cell proliferation and killing pancreatic cancer cells were measured by CCK-8 assay. Perforin, granzyme B (Gran B), CD107a, and NKG2D expressions of NK cells induced with apigenin were detected by flow cytometry (FCM). The mRNA expression of Bcl-2, Bax and protein expression of Bcl-2, Bax, p-ERK, and p-JNK in NK cells were evaluated by qRT-PCR and western blotting analysis, respectively. The results showed that appropriate concentration of apigenin could significantly promote the proliferation of NK cells in vitro and enhance the killing activity of NK cells against pancreatic cancer cells. The expressions of surface antigen NKG2D and intracellular antigen perforin and Gran B of NK cells were upregulated after treating with apigenin. Bcl-2 mRNA expression was increased, while Bax mRNA expression was decreased. Similarly, the expression of Bcl-2, p-JNK, and p-ERK protein was upregulated, and the expression of Bax protein was downregulated. The molecular mechanism of the immunopotentiation effects of apigenin may be that it up-regulates Bcl-2 and down-regulates Bax expression at the gene and protein levels to facilitate NK cell proliferation, and up-regulates the expression of perforin, Gran B, and NKG2D through the activation of JNK and ERK pathways to enhance NK cell cytotoxicity.

Indexed as

ApigeninPancreatic Neoplasmsbcl-2-Associated X ProteinCell ProliferationHumansNatural Killer T-CellsNK Cell Lectin-Like Receptor Subfamily KPerforinProto-Oncogene Proteins c-bcl-2RNA, MessengerApigeninbcl-2-Associated X ProteinNK Cell Lectin-Like Receptor Subfamily KPerforinProto-Oncogene Proteins c-bcl-2RNA, MessengerApigeninimmunopotentiationkilling activityNK cellpancreatic cancer

Identifiers

PMID36848930
PMCPMC9974612
OpenAlexW4322422814

What OpenQuestion holds

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LicenceCC BY-NC
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.