Evidence map›Paper›PMID 31295843›Full record

ArticleInternational journal of molecular sciences2019

Inhibition of Phosphatidylinositol 3-kinase (PI3K) Signaling Synergistically Potentiates Antitumor Efficacy of Paclitaxel and Overcomes Paclitaxel-Mediated Resistance in Cervical Cancer.

Jing Jing Liu, Jung Yoon Ho, Hye Won Lee, Min Wha Baik, Oyoung Kim, Youn Jin Choi, Soo Young Hur

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

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  17. Translational cancer research · 2020
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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

7 authors at 2 institutions in 1 country.

Jing Jing LiuDepartment of Gynecology and Obstetrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea.
Jung Yoon HoDepartment of Gynecology and Obstetrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea.
Hye Won LeeDepartment of Health Sciences and Technology, SAIHST, Sungkyunkwan University, Seoul 06591, Korea.
Min Wha BaikDepartment of Gynecology and Obstetrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea.
Oyoung KimDepartment of Gynecology and Obstetrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea.
Youn Jin ChoiDepartment of Gynecology and Obstetrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea. yunno@catholic.ac.kr.ORCID 0000-0003-4699-2116
Soo Young HurDepartment of Gynecology and Obstetrics, Seoul St. Mary's Hospital, The Catholic University of Korea, Seoul 06591, Korea. hursy@catholic.ac.kr.
The Catholic University of Korea Seoul St. Mary's Hospital · KRSungkyunkwan University · KR

Funding

Bio & Medical Technology Development Program of the National Research Foundation (NRF) funded by the Ministry of Science & ICT 2018M3A9E8021512National Research Foundation of Korea 2016R1D1A1B04932862
6 · The paper itself

Abstract

Acquired paclitaxel (PTX) resistance limits its effectiveness and results in advanced cancer progression. This review investigated whether the inhibition of phosphatidylinositol 3-kinase (PI3K) signaling overcomes paclitaxel resistance in cervical cancer. It was established paclitaxel-resistant cell lines (PTX-R ME180/PTX-R HeLa) and determined the combination index for paclitaxel and PI3K inhibitors (BYL-719/ LY294002) by tetrazolium dye assay. Flow cytometry was used to detect the cell cycle and apoptosis. Migration and invasion were explored by wound healing and transwell assays. Genes related to multiple pathways were assessed by a western blot. It was found that the PI3K pathway was significantly activated in paclitaxel-resistant HeLa and ME180 cells compared to parental cells. PTX + PI3K inhibitor combined therapy showed a synergistic effect by strengthening paclitaxel-induced S and G

Indexed as

Antineoplastic AgentsApoptosisCell CycleCell Line, TumorClass I Phosphatidylinositol 3-KinasesDNA DamageDrug Resistance, NeoplasmDrug SynergismEnzyme InhibitorsFemaleGenetic VariationHumansPaclitaxelPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktSignal TransductionAntineoplastic AgentsClass I Phosphatidylinositol 3-KinasesEnzyme InhibitorsPaclitaxelPhosphatidylinositol 3-KinasePIK3CA protein, humanProto-Oncogene Proteins c-aktcell cyclecervical cancercombination therapyinvasionpaclitaxel resistancePI3K inhibitor

Identifiers

PMID31295843
PMCPMC6679163
OpenAlexW2960589694

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.