Evidence map›Paper›PMID 27634890›Full record

ArticleOncotarget2016

Epigenetic therapy potential of suberoylanilide hydroxamic acid on invasive human non-small cell lung cancer cells.

Shirong Zhang, Kan Wu, Jianguo Feng, Zhibing Wu, Qinghua Deng, Chao Guo, Bing Xia, Jing Zhang, Haixiu Huang, Lucheng Zhu and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 6 institutions in 2 countries.

Shirong ZhangDepartment of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, Hangzhou, China.
Kan WuDepartment of Oncology, Affiliated Hangzhou First People's Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Jianguo FengCancer Research institute, Zhejiang Cancer Hospital, Hangzhou, China.
Zhibing WuDepartment of Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
Qinghua DengDepartment of Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
Chao GuoDepartment of Cancer Genetics and Epigenetics, City of Hope National Medical Center, Duarte, CA, USA.
Bing XiaDepartment of Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
Jing ZhangDepartment of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, Hangzhou, China.
Haixiu HuangDepartment of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, Hangzhou, China.
Lucheng ZhuDepartment of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, Hangzhou, China.
Ke ZhangDepartment of Oncology, Hangzhou Cancer Hospital, Hangzhou, China.
Binghui ShenDepartment of Cancer Genetics and Epigenetics, City of Hope National Medical Center, Duarte, CA, USA.
Xufeng ChenDepartment of Pathology and Laboratory Medicine, University of California at Los Angeles, Los Angeles, CA, USA.
Shenglin MaDepartment of Oncology, Hangzhou First People's Hospital, Nanjing Medical University, Hangzhou, China.
Hangzhou First People's Hospital · CNHangzhou Cancer Hospital · CNCancer Genetics (United States) · USCity Of Hope National Medical Center · USUniversity of California, Los Angeles · USZhejiang Cancer Hospital · CN

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
Role of Nucleases in RNA Primer Removal and MutagenesisR01CA085344 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI SHEN, BINGHUI · 1999 to 2024
$7.7M
NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA085344
6 · The paper itself

Abstract

Metastasis is the reason for most cancer death, and a crucial primary step for cancer metastasis is invasion of the surrounding tissue, which may be initiated by some rare tumor cells that escape the heterogeneous primary tumor. In this study, we isolated invasive subpopulations of cancer cells from human non-small cell lung cancer (NSCLC) H460 and H1299 cell lines, and determined the gene expression profiles and the responses of these invasive cancer cells to treatments of ionizing radiation and chemotherapeutic agents. The subpopulation of highly invasive NSCLC cells showed epigenetic signatures of epithelial-mesenchymal transition, cancer cell stemness, increased DNA damage repair and cell survival signaling. We also investigated the epigenetic therapy potential of suberoylanilide hydroxamic acid (SAHA) on invasive cancer cells, and found that SAHA suppresses cancer cell invasiveness and sensitizes cancer cells to treatments of IR and chemotherapeutic agents. Our results provide guidelines for identification of metastatic predictors and for clinical management of NSCLC. This study also suggests a beneficial clinical potential of SAHA as a chemotherapeutic agent for NSCLC patients.

Indexed as

Epigenesis, GeneticAnimalsAntineoplastic AgentsApoptosisCarcinoma, Non-Small-Cell LungCell DifferentiationCell Line, TumorCell SurvivalDNA DamageDNA RepairEpithelial-Mesenchymal TransitionFemaleHistone Deacetylase InhibitorsHumansHydroxamic AcidsLung NeoplasmsAntineoplastic AgentsHistone Deacetylase InhibitorsHydroxamic AcidsVorinostatepigeneticsepigenetic therapyinvasionnon-small cell lung cancersuberoylanilide hydroxamic acid

Identifiers

PMID27634890
PMCPMC5356588
OpenAlexW2520278398

What OpenQuestion holds

Textmetadata
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.