Evidence map›Paper›PMID 32440210›Full record

ArticleCancer management and research2020

Active Monomer RTR-1 Derived from the Root of

Xiangqiang Zhang, Jinxia Cheng, Peiyan He, Jinyan Zhu, Zhixian Chen, Shenyu Miao, Guocai Wang, Jianwei Jiang, Yuechun Wang

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Review
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

9 authors at 3 institutions in 1 country.

Xiangqiang Zhang *Department of Physiology, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.
Jinxia Cheng *Department of Physiology, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.ORCID 0000-0001-8184-6144
Peiyan HeDepartment of Biochemistry, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.
Jinyan ZhuDepartment of Immunology, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.
Zhixian ChenDepartment of Biochemistry, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.
Shenyu MiaoSchool of Life Sciences, Guangzhou University, Guangzhou, People's Republic of China.
Guocai WangInstitute of Traditional Chinese Medicine and Natural Products, College of Pharmacy, Jinan University, Guangzhou 510630, People's Republic of China.
Jianwei JiangDepartment of Biochemistry, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.ORCID 0000-0001-7246-6924
Yuechun WangDepartment of Physiology, Basic Medical College, Jinan University, Guangzhou 510630, People's Republic of China.
Jinan University · CNGuangzhou University · CNShandong University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose

methodsCell proliferation was determined by MTT and clone formation assay. The effect of RTR-1 on cell cycle distribution and apoptosis was analysed utilizing flow cytometry, respectively. Moreover, Western blotting was used to detect the expression of cell cycle- and apoptosis-related protein.

resultsBased on MTT and clone formation assay, we noticed that RTR-1 inhibited the proliferation of gastric carcinoma (BGC823 and SGC7901) cells in a dose- and time-dependent manner. Furthermore, the results of flow cytometry and Western blotting showed that RTR-1 induced cell cycle arrest in the G2/M phase through the ATM-Chk2-p53-p21 signaling pathway and induced cell apoptosis by inhibiting the signal transducers and activators of transcription 3 (STAT3) pathway and activating the endoplasmic reticulum stress (ER stress) pathway.

conclusionTaken together, these results demonstrate that RTR-1 induces cell cycle arrest and promotes apoptosis in gastric carcinoma, indicating its potential application for gastric cancer therapy.

Indexed as

apoptosiscell cycleER stressgastric carcinoma cellsRTR-1STAT3

Identifiers

PMID32440210
PMCPMC7211317
OpenAlexW3023845373

What OpenQuestion holds

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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.