Evidence map›Paper›PMID 31084542›Full record

ArticleJournal of medicinal food2019

Sulforaphane Decrease of SERTAD1 Expression Triggers G1/S Arrest in Breast Cancer Cells.

An-Chin Cheng, Ching-Ju Shen, Chao-Ming Hung, Yi-Chiang Hsu

Open access · hybridAbstract read
In one paragraph

Article in Journal of medicinal food, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 32 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

4 authors at 4 institutions in 2 countries.

An-Chin Cheng1 Department of Nutrition and Health Sciences; College of Health Sciences; Chang Jung Christian University, Tainan, Taiwan.
Ching-Ju Shen2 Department of Gynecology and Obstetrics, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
Chao-Ming Hung3 Department of General Surgery, E-Da Hospital, I-Shou University, Kaohsiung, Taiwan.
Yi-Chiang Hsu4 Department of Medical Sciences Industry, College of Health Sciences; Chang Jung Christian University, Tainan, Taiwan.
Chang Jung Christian University · TWCollege of Medical Sciences · NPE-Da Hospital · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies have identified the potential of chemopreventive effects of sulforaphane (SFN); however, the underlying mechanisms of its effect on breast cancer require further elucidation. This study investigated the anticancer effects of SFN that specifically induces G1/S arrest in breast ductal carcinoma (ZR-75-1) cells. The proliferation of the cancer cells after treatment with SFN was detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. DNA content and cell cycle status were analyzed through flow cytometry. Our results demonstrated the inhibition of growth in ZR-75-1 cells upon SFN exposure. In addition, SERTAD1 (SEI-1) caused the accumulation of SFN-treated G1/S-phase cells. The downregulation of SEI-1, cyclin D2, and histone deacetylase 3 suggested that in addition to the identified effects of SFN against breast cancer prevention, it may also exert antitumor activities in established breast cancer cells. In conclusion, SFN can inhibit growth of and induce cell cycle arrest in cancer cells, suggesting its potential role as an anticancer agent.

Indexed as

Antineoplastic Agents, PhytogenicBreast NeoplasmsCell Line, TumorCell ProliferationCyclin D2G1 Phase Cell Cycle CheckpointsHistone Deacetylase 3Histone DeacetylasesHumansIsothiocyanatesNuclear ProteinsPlant ExtractsS Phase Cell Cycle CheckpointsSulfoxidesTrans-ActivatorsTranscription FactorsAntineoplastic Agents, PhytogenicCyclin D2Histone Deacetylase 3Histone DeacetylasesIsothiocyanatesNuclear ProteinsPlant ExtractsSERTAD1 protein, humansulforaphaneSulfoxidesTrans-ActivatorsTranscription Factors

Identifiers

PMID31084542
PMCPMC6534085
OpenAlexW2946812414

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.