Evidence map›Paper›PMID 30358009›Full record

ReviewCancer science2019

Novel application of metformin combined with targeted drugs on anticancer treatment.

Jun Deng, Mei Peng, Zhiren Wang, Sichun Zhou, Di Xiao, Jiating Deng, Xue Yang, Jingyuan Peng, Xiaoping Yang

Open access · goldAbstract readReview
In one paragraph

Review in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
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  7. Landscape of targeted therapies for advanced urothelial carcinoma.Exploration of targeted anti-tumor therapy · 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

9 authors at 2 institutions in 1 country.

Jun DengKey Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, School of Medicine, Hunan Normal University, Changsha, Hunan, China.ORCID http://orcid.org/0000-0003-4931-3246
Mei PengDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Zhiren WangKey Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, School of Medicine, Hunan Normal University, Changsha, Hunan, China.
Sichun ZhouKey Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, School of Medicine, Hunan Normal University, Changsha, Hunan, China.
Di XiaoKey Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, School of Medicine, Hunan Normal University, Changsha, Hunan, China.
Jiating DengKey Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, School of Medicine, Hunan Normal University, Changsha, Hunan, China.
Xue YangDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jingyuan PengDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Xiaoping YangKey Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, School of Medicine, Hunan Normal University, Changsha, Hunan, China.
Central South University · CNHunan Normal University · CN

Funding

Hunan Natural Science Foundation 2016JJ2187Hunan Provincial Natural Science Foundation 2018JJ3831Institutional Fund of Xiangya Hospital Central South University 2016Q02Key Project of Hunan Province 2016 2016JC2036National Natural Science Foundation of China 81703008National Natural Science Foundation of China 81874212Start-up Funds of the Key Laboratory of Study and Discovery of Targeted Small Molecules of Hunan Province 2017TP1020
6 · The paper itself

Abstract

The success of targeted drug therapies for treating cancer patients has attracted broad attention both in the academic community and social society. However, rapidly developed acquired resistance is becoming a newly recognized major challenge to the continuing efficiency of these therapies. Metformin is a well-known natural compound with low toxicity derived from the plant French lilac. Our previous work has highlighted research progress of the combination of clinically applied chemotherapies and metformin by different mechanisms. We have also launched a study to combine metformin with the small molecule targeted drug gefitinib to treat bladder cancer using intravesical administration. Thus, in this minireview, we summarize recent achievements combining metformin with various targeted therapies. This work directs the potential clinical future by selecting available cancer patients and providing precise medicine by the combination of metformin and targeted drugs to overcome resistance and enhance therapeutic efficacies.

Indexed as

Administration, IntravesicalAntineoplastic Combined Chemotherapy ProtocolsDrug Resistance, NeoplasmGefitinibHumansMetforminMolecular Targeted TherapyTreatment OutcomeUrinary Bladder NeoplasmsGefitinibMetformincombinationmetforminsmall molecular inhibitorsynergistic effecttargeted therapy

Identifiers

PMID30358009
PMCPMC6317954
OpenAlexW2898141131

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.