Evidence map›Paper›PMID 27834342›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2016

Allyl Isothiocyanate Inhibits the Proliferation of Renal Carcinoma Cell Line GRC-1 by Inducing an Imbalance Between Bcl2 and Bax.

Zhongyong Jiang, Xi Liu, Kai Chang, Xia Liu, Jie Xiong

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Peripheral CD4Journal of biomedical research · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Effects of ASPP2 on proliferation and apoptosis of malignant spinal tumor cells.International journal of clinical and experimental pathology · 2017
    Article
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 1 institution in 1 country.

Zhongyong JiangDepartment of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Xi LiuMedical Department, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Kai ChangDepartment of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Xia LiuDepartment of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Jie XiongDepartment of Clinical Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan, China (mainland).
Chengdu Military General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Because of the insensitivity of renal cell carcinoma (RCC) to both chemotherapy and radiotherapy, surgery remains the primary approach for anticancer treatment. However, patients who do not receive timely diagnoses may not be suitable for surgery, especially in the late phase of tumor development. Thus, the discovery of novel effective treatment is of great importance. Allyl isothiocyanate (AITC) can inhibit the proliferation and induce apoptosis in many cancer cells. In this paper, we report on an in vitro study to determine the effect of AITC on proliferation and apoptosis of RCC line GRC-1. MATERIAL AND METHODS CCK8 assay was used to detect cell proliferation under gradient concentrations of AITC. Flow cytometry was employed to evaluate cell apoptosis. Real-time fluorescent polymerase chain reaction quantified mRNA levels of Bax and Bcl-2 genes. Western blotting was further employed for protein expression assay. RESULTS AITC inhibited GRC-1 cell proliferation and induced cell apoptosis in a dose-dependent manner; it also elevated Bax while suppressing Bcl-2 gene expression at both mRNA and protein levels. In general, increasing concentration of AITC decreased Bcl-2/Bax ratio. CONCLUSIONS The inhibitory effect of AITC on GRC-1 cells is exerted via cell apoptosis, in which the imbalance of Bcl-2/Bax plays a significant role.

Indexed as

AdultApoptosisbcl-2-Associated X ProteinCarcinoma, Renal CellCell Line, TumorCell ProliferationGenes, bcl-2HumansIsothiocyanatesKidney NeoplasmsMaleProto-Oncogene Proteins c-bcl-2allyl isothiocyanateBAX protein, humanbcl-2-Associated X ProteinBCL2 protein, humanIsothiocyanatesProto-Oncogene Proteins c-bcl-2AlprenololApoptosis Inducing FactorCellulose 1,4-beta-Cellobiosidase

Identifiers

PMID27834342
PMCPMC5115214
OpenAlexW2555133689

What OpenQuestion holds

Textmetadata
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.