Evidence map›Paper›PMID 30488540›Full record

ArticleCancer science2019

Augmented antitumor activity of 5-fluorouracil by double knockdown of MDM4 and MDM2 in colon and gastric cancer cells.

Mamiko Imanishi, Yoshiyuki Yamamoto, Xiaoxuan Wang, Akinori Sugaya, Mitsuaki Hirose, Shinji Endo, Yukikazu Natori, Kenji Yamato, Ichinosuke Hyodo

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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  10. Association ofPharmacogenomics and personalized medicine · 2020
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  11. Observational
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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

9 authors at 4 institutions in 1 country.

Mamiko ImanishiDepartment of Gastroenterology and Hepatology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Yoshiyuki YamamotoDepartment of Gastroenterology and Hepatology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Xiaoxuan WangDepartment of Gastroenterology and Hepatology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Akinori SugayaDepartment of Gastroenterology, Kasumigaura Medical Center, Tsuchiura, Japan.
Mitsuaki HiroseDepartment of Gastroenterology, Tsuchiura Clinical Education and Training Center, University of Tsukuba Hospital, Tsuchiura, Japan.
Shinji EndoDepartment of Gastroenterology and Hepatology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
Yukikazu NatoriRNAi Company Ltd., Bunkyo-ku, Japan.
Kenji YamatoDepartment of Gastroenterology and Hepatology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.ORCID https://orcid.org/0000-0003-4990-9891
Ichinosuke HyodoDepartment of Gastroenterology and Hepatology, Institute of Clinical Medicine, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Japan.
University of Tsukuba · JPBunkyo University · JPKasumigaura Medical Center · JPTsuchiura Kyodo General Hospital · JP

Funding

Ministry of Education, Culture, Sports, Science and Technology of Japan 26460624
6 · The paper itself

Abstract

Inactivation of the TP53 tumor suppressor gene is essential during cancer development and progression. Mutations of TP53 are often missense and occur in various human cancers. In some fraction of wild-type (wt) TP53 tumors, p53 is inactivated by upregulated murine double minute homolog 2 (MDM2) and MDM4. We previously reported that simultaneous knockdown of MDM4 and MDM2 using synthetic DNA-modified siRNAs revived p53 activity and synergistically inhibited in vitro cell growth in cancer cells with wt TP53 and high MDM4 expression (wtTP53/highMDM4). In the present study, MDM4/MDM2 double knockdown with the siRNAs enhanced 5-fluorouracil (5-FU)-induced p53 activation, arrested the cell cycle at G

Indexed as

AnimalsAntineoplastic AgentsCell Cycle ProteinsCell Line, TumorCell ProliferationColonic NeoplasmsFemaleFluorouracilG1 PhaseGene Expression Regulation, NeoplasticHCT116 CellsHumansMiceMice, Inbred BALB CMice, NudeNuclear ProteinsAntineoplastic AgentsCell Cycle ProteinsFluorouracilMDM2 protein, humanMDM4 protein, humanNuclear ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p535-fluorouracilcolon cancergastric cancerMDM4p53

Identifiers

PMID30488540
PMCPMC6361612
OpenAlexW2902757789

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.