Evidence map›Paper›PMID 30949414›Full record

ArticleAmerican journal of cancer research2019

Synergism of PARP inhibitor fluzoparib (HS10160) and MET inhibitor HS10241 in breast and ovarian cancer cells.

Ye Han, Mei-Kuang Chen, Hung-Ling Wang, Jennifer L Hsu, Chia-Wei Li, Yu-Yi Chu, Chun-Xiao Liu, Lei Nie, Li-Chuan Chan, Clinton Yam and 5 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 33 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

15 authors at 1 institution in 1 country.

Ye HanDepartment of Second Breast Surgery, China Medical University Affiliated Shengjing Hospital Shenyang, P. R. China.
Mei-Kuang ChenDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Hung-Ling WangGraduate Institute of Biomedical Sciences, College of Medicine, China Medical University Taichung 40402, Taiwan.
Jennifer L HsuDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Chia-Wei LiDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Yu-Yi ChuDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Chun-Xiao LiuDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Lei NieDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Li-Chuan ChanDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Clinton YamDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Shao-Chun WangGraduate Institute of Biomedical Sciences, College of Medicine, China Medical University Taichung 40402, Taiwan.
Gui-Jin HeDepartment of Second Breast Surgery, China Medical University Affiliated Shengjing Hospital Shenyang, P. R. China.
Gabriel N HortobagyiDepartment of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
Xiao-Dong TanDepartment of Thyroid and Pancreatic Surgery, China Medical University Affiliated Shengjing Hospital Shenyang, P. R. China.
Mien-Chie HungDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Mechanical Drugs: Harnessing Cancer Aggressiveness to Overcome Its ResistanceU01CA201777 · NCI · MASIMO CORPORATION · PI NAULI, SURYA, SHARMA, VIKRANT · 2016 to 2020
$2.4M
Rational Combination Therapy with PARP Inhibitors in Triple Negative Breast CancerR01CA211615 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YANG, LIUQING · 2017 to 2021
$2.1M
Training Grant in Cancer BiologyT32CA186892 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KALLURI, RAGHU · 2016 to 2020
$1.1M
NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA211615NCI NIH HHS T32 CA186892NCI NIH HHS U01 CA201777
6 · The paper itself

Abstract

Poly (ADP-ribose) polymerase (PARP) inhibitors (PARPi) are promising targeted therapeutics for breast and ovarian cancers bearing a germline

Indexed as

high-grade serous ovarian cancerMETPARPresistanceSHR-3162Targeted therapytriple-negative breast cancer

Identifiers

PMID30949414
PMCPMC6448061
OpenAlexW2981086035

What OpenQuestion holds

Textmetadata
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.