Evidence map›Paper›PMID 31348594›Full record

ArticleCancer science2019

Silent mating-type information regulation 2 homolog 1 overexpression is an important strategy for the survival of adapted suspension tumor cells.

Ji Young Park, Sora Han, Hye In Ka, Hyun Jeong Joo, Su Jung Soh, Kyung Hyun Yoo, Young Yang

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 13 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

7 authors at 1 institution in 1 country.

Ji Young ParkDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.
Sora HanDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.
Hye In KaDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.
Hyun Jeong JooDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.
Su Jung SohDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.
Kyung Hyun YooDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.
Young YangDepartment of Biological Sciences, Research Center for Cellular Heterogeneity, Research Institute of Women's Health, Sookmyung Women's University, Seoul, Korea.ORCID https://orcid.org/0000-0001-8975-5087
Sookmyung Women's University · KR

Funding

Ministry of Science, ICT and Future Planning NRF-2016R1A5A1011974
6 · The paper itself

Abstract

Characterization of circulating tumor cells (CTC) is important to prevent death caused by the metastatic spread of cancer cells because CTC are associated with distal metastasis and poor prognosis of breast cancer. We have previously developed suspension cells (SC) using breast cancer cell lines and demonstrated their high metastatic potential. As survival of CTC is highly variable from a few hours to decades, herein we cultured SC for an extended time and named them adapted suspension cells (ASC). Silent mating-type information regulation 2 homolog 1 (SIRT1) expression increased in ASC, which protected the cells from apoptosis. High SIRT1 expression was responsible for the suppression of nuclear factor kappa B (NF-κB) activity and downregulation of reactive oxygen species (ROS) in ASC. As the inhibition of NF-κB and ROS production in SIRT1-depleted ASC contributed to the development of resistance to apoptotic cell death, maintenance of a low ROS level and NF-κB activity in ASC is a crucial function of SIRT1. Thus, SIRT1 overexpression may play an important role in growth adaptation of SC because SIRT1 expression is increased in long-term rather than in short-term cultures.

Indexed as

Cell SurvivalAnimalsApoptosisBreast NeoplasmsCell Line, TumorDown-RegulationFemaleGene Expression Regulation, NeoplasticHumansMiceNeoplastic Cells, CirculatingNF-kappa BReactive Oxygen SpeciesSignal TransductionSirtuin 1Xenograft Model Antitumor AssaysNF-kappa BReactive Oxygen SpeciesSIRT1 protein, humanSirtuin 1adapted suspension cellcirculating tumor cellNF-κBreactive oxygen speciesSIRT1

Identifiers

PMID31348594
PMCPMC6726698
OpenAlexW2966534982

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.