Evidence map›Paper›PMID 29750041›Full record

ArticleOncoTargets and therapy2018

Peptide SA12 inhibits proliferation of breast cancer cell lines MCF-7 and MDA-MB-231 through G0/G1 phase cell cycle arrest.

Longfei Yang, Huanran Liu, Min Long, Xi Wang, Fang Lin, Zhaowei Gao, Huizhong Zhang

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Future in the Past:International journal of molecular sciences · 2018
    Article
  3. 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

7 authors at 2 institutions in 1 country.

Longfei Yang *Department of Medical Laboratory and Research Center, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Huanran Liu *Department of General Surgery, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Min LongDepartment of Medical Laboratory and Research Center, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Xi WangDepartment of Medical Laboratory and Research Center, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Fang LinDepartment of Medical Laboratory and Research Center, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Zhaowei GaoDepartment of Medical Laboratory and Research Center, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Huizhong ZhangDepartment of Medical Laboratory and Research Center, Tangdu Hospital, Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CNFirst Affiliated Hospital of Dalian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTargeted therapies have been proven as promising in the treatment of breast cancer and have improved survival and quality of life in advanced breast cancer. We previously identified a novel peptide SA12 which showed significant activity in the inhibition of proliferation and induction of apoptosis in SKBr-3 cells.

methodsThe present study investigated the potential antitumor role of SA12 in breast cancer cell lines MDA-MB-231 and MCF-7 through Cell Counting Kit-8 assay and colony formation assay, and examined the cell cycle distribution using flow cytometry analysis. Furthermore, the expression of cell cycle-related genes

resultsWe determined that peptide SA12 suppressed the proliferation of MDA-MB-231 and MCF-7 cell lines through the G0/G1 phase cell cycle arrest. Moreover, the expressions of cell cycle-associated genes

conclusionWe concluded that SA-12 inhibits the proliferation of MCF-7 and MDA-MB-231 cells through G0/G1 cell cycle arrest. Cell cycle related genes

Indexed as

breast cancerCDK4cyclin D1G0/G1 arrestp16SA12

Identifiers

PMID29750041
PMCPMC5935185
OpenAlexW2802322851

What OpenQuestion holds

Textmetadata
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.