Evidence map›Paper›PMID 27484466›Full record

ArticleBMC cancer2016

Inhibition of nuclear factor-kappa B enhances the tumor growth of ovarian cancer cell line derived from a low-grade papillary serous carcinoma in p53-independent pathway.

Xue Xiao, Gong Yang, Peng Bai, Shunping Gui, Tri M Bui Nyuyen, Imelda Mercado-Uribe, Mei Yang, Juan Zou, Qintong Li, Jianguo Xiao and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Targeting BCL-xL in Myeloid Malignancies: From Inhibitors to PROTAC.Journal of cellular and molecular medicine · 2026
    Review
  2. The cross-talk between GSK-3β, RKIP, and PTEN as potential targets for therapeutic implications in cancer: a comprehensive insight.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
  3. Methanolic Leaves Extract ofInternational journal of molecular sciences · 2025
    Article
  4. Article
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  6. LKB1 biology: assessing the therapeutic relevancy of LKB1 inhibitors.Cell communication and signaling : CCS · 2024
    Review
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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

14 authors at 5 institutions in 2 countries.

Xue XiaoDepartment of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Gong YangCancer Research Laboratory, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Peng BaiWest China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, 610041, People's Republic of China.
Shunping GuiDepartment of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Tri M Bui NyuyenDepartment of Biochemistry and Molecular Biology, George Washington University, Washington, D.C., USA.
Imelda Mercado-UribeDepartment of Pathology, University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Mei YangDepartment of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Juan ZouDepartment of Pathology, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Qintong LiDepartment of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Jianguo XiaoDepartment of Pathology, University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
Bin ChangDepartment of Pathology, Shihezi University School of Medicine, Shihezi, Xinjiang, 82002, China.
Guangzhi LiuDepartment of Pathology, University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.
He WangDepartment of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, 610041, People's Republic of China. wanghe_cd@126.com.
Jinsong LiuDepartment of Pathology, University of Texas M. D. Anderson Cancer Center, Houston, TX, USA. 19811454@qq.com.
Sichuan University · CNThe University of Texas MD Anderson Cancer Center · USGeorge Washington University · USShanghai Medical College of Fudan University · CNShihezi University · CN

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Therapeutic Micro RNA Strategies for Ovarian CancerP50CA083638 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GODWIN, ANDREW K., GOLEMIS, ERICA A. · 1999 to 2013
$33.6M
RAS Signaling, Senescent Fibroblasts, and Ovarian Cancer ProgressionR01CA131183 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIU, JINSONG · 2008 to 2012
$1.3M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA083638NCI NIH HHS R01 CA131183
6 · The paper itself

Abstract

backgroundNF-kB can function as an oncogene or tumor suppressor depending on cancer types. The role of NF-kB in low-grade serous ovarian cancer, however, has never been tested. We sought to elucidate the function of NF-kB in the low-grade serous ovarian cancer.

methodsThe ovarian cancer cell line, HOC-7, derived from a low-grade papillary serous carcinoma. Introduction of a dominant negative mutant, IkBαM, which resulted in decrease of NF-kB function in ovarian cancer cell lines. The transcription ability, tumorigenesis, cell proliferation and apoptosis were observed in derivative cell lines in comparison with parental cells.

resultsWestern blot analysis indicated increased expression of the anti-apoptotic proteins Bcl-xL and reduced expression of the pro-apoptotic proteins Bax, Bad, and Bid in HOC-7/IĸBαM cell. Further investigations validate this conclusion in KRAS wildtype cell line SKOV3. Interesting, NF-kB can exert its pro-apoptotic effect by activating mitogen-activated protein kinase (MAPK) phosphorylation in SKOV3 ovarian cancer cell, whereas opposite changes detected in p-MEK in HOC-7 ovarian cancer cell, the same as some chemoresistant ovarian cancer cell lines. In vivo animal assay performed on BALB/athymic mice showed that injection of HOC-7 induced subcutaneous tumor growth, which was completely regressed within 7 weeks. In comparison, HOC-7/IĸBαM cells caused sustained tumor growth and abrogated tumor regression, suggesting that knock-down of NF-kB by IĸBαM promoted sustained tumor growth and delayed tumor regression in HOC-7 cells.

conclusionOur results demonstrated that NF-kB may function as a tumor suppressor by facilitating regression of low grade ovarian serous carcinoma through activating pro-apoptotic pathways.

Indexed as

AnimalsApoptosisbcl-X ProteinCarcinoma, Ovarian EpithelialCell Line, TumorCell ProliferationCystadenocarcinoma, SerousFemaleHumansMiceNeoplasms, Glandular and EpithelialNeoplasm TransplantationNF-kappa BNF-KappaB Inhibitor alphaOvarian NeoplasmsPhosphorylationBCL2L1 protein, humanbcl-X ProteinNF-kappa BNF-KappaB Inhibitor alphaNFKBIA protein, humanTumor Suppressor Protein p53IkBαMNF-kBOvarian cancerPro-apoptosisTumor suppressor

Identifiers

PMID27484466
PMCPMC4971665
OpenAlexW2500446133

What OpenQuestion holds

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LicenceCC BY
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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.