Evidence map›Paper›PMID 36254198›Full record

ArticleJournal of immunology research2022

Jujuboside B Reverse CUMS-Promoted Tumor Progression via Blocking PI3K/Akt and MAPK/ERK and Dephosphorylating CREB Signaling.

Zhen Yang, Weijia Cai, Yitian Chen, Zhijun Guo, Zhijun Xiao, Ting Zhou, Yuanchi Cheng, Feng Xu

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Zhen YangFengxian Hospital, Southern Medical University, Shanghai 201499, China.ORCID https://orcid.org/0000-0003-2105-3630
Weijia CaiFengxian Hospital, Southern Medical University, Shanghai 201499, China.
Yitian ChenFengxian Hospital, Southern Medical University, Shanghai 201499, China.
Zhijun GuoFengxian Hospital, Southern Medical University, Shanghai 201499, China.
Zhijun XiaoSixth People's Hospital South Campus, Shanghai Jiao Tong University, Shanghai 201499, China.
Ting ZhouSixth People's Hospital South Campus, Shanghai Jiao Tong University, Shanghai 201499, China.
Yuanchi ChengFengxian Hospital, Southern Medical University, Shanghai 201499, China.ORCID https://orcid.org/0000-0002-8166-4559
Feng XuFengxian Hospital, Southern Medical University, Shanghai 201499, China.ORCID https://orcid.org/0000-0001-6215-8696
Southern Medical University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Jujuboside B (JUB) is a saponins isolated from the seeds of Methods: 56 female C57BL/6 mice were grouped into 7 groups: A (blank control), B (tumor-bearing control), C (tumor-bearing + JUB), D (CUMS control), E (CUMS + JUB), F (tumor-bearing + CUMS), and G (tumor-bearing + CUMS + JUB). Groups C, E, G, B, D, and F were administered, respectively, with JUB (40 mg/kg/day) or vehicle for 2 weeks. Serum 5-HT, Trp (tryptophane), inflammatory cytokines TNF- Results: Chronic stress successfully induced the depression-like phenotype (group D vs. A) and promoted tumor growth (group B vs. F). JUB significantly ameliorated the depression-like phenotype and increased 5-HT, Trp levels (group D vs. E), and reversing CUMS-induced tumor progression. Meanwhile, JUB decreased inflammatory cytokine levels. Chronic stress upregulated the phosphorylation levels of PI3K/Akt/MAPK/ERK/CREB; JUB reversed this regulation. JUB significantly inhibited cell viability, colony formation rate, and downregulated the phosphorylation levels of PI3K/Akt/MAPK/ERK/CREB in vitro. Conclusions: JUB reverses CUMS-promoted tumor progression in tumor-bearing mice with depression-like phenotype. JUB exerts the dual beneficial effect on tumor growth and depression-like phenotype by blocking the signal transduction pathway of PI3K/Akt, MAPK/ERK, and dephosphorylating the downstream signaling regulator CREB.

Indexed as

Phosphatidylinositol 3-KinasesSaponinsAnimalsAntidepressive Agentsbcl-2-Associated X ProteinCytokinesFemaleInterleukin-4MiceMice, Inbred C57BLProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2RNA, MessengerSerotoninSignal TransductionTumor Necrosis Factor-alphaAntidepressive Agentsbcl-2-Associated X ProteinCytokinesInterleukin-4jujuboside BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2RNA, MessengerSaponinsSerotoninTumor Necrosis Factor-alpha

Identifiers

PMID36254198
PMCPMC9569198
OpenAlexW4303648084

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.