Evidence map›Paper›PMID 33507584›Full record

ArticleJournal of cellular and molecular medicine2021

Potent antitumour of the mTORC1/2 dual inhibitor AZD2014 in docetaxel-sensitive and docetaxel-resistant castration-resistant prostate cancer cells.

Senmao Li, Jindong Sheng, Zhenhua Liu, Yu Fan, Cuijian Zhang, Tianjing Lv, Shuai Hu, Jie Jin, Wei Yu, Yi Song

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 28 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

10 authors at 2 institutions in 1 country.

Senmao LiDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.ORCID 0000-0003-0377-8566
Jindong ShengDepartment of Gynaecological Oncology, Key Laboratory of Cancer Prevention and Therapy of Tianjin, Tianjin's Clinical Research Center for Cancer, National Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Zhenhua LiuDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Yu FanDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Cuijian ZhangDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Tianjing LvDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Shuai HuDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Jie JinDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Wei YuDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Yi SongDepartment of Urology, Beijing Key Laboratory of Urogenital Diseases (Male), Molecular Diagnosis and Treatment Center, National Research Center for Genitourinary Oncology, Peking University First Hospital and Institute of Urology, Peking University, Beijing, China.
Peking University · CNTianjin Medical University Cancer Institute and Hospital · CN

Funding

AstraZeneca Company C-2016-004National Natural Science Foundation of China 81770755National Natural Science Foundation of China 81870518Natural Science Foundation of Beijing Municipality 7192208
6 · The paper itself

Abstract

Recent studies indicate mammalian target of rapamycin (mTOR) may play an important role in PCa progression and drug resistance. Here, we investigated the effects of a novel mTORC1/C2 dual inhibitor, AZD2014, on naive and docetaxel (Doc)-pre-treated castration-resistant PCa (CRPC) cells and explored its therapeutic potential in CRPCs. In the current study, AZD2014 has a greater inhibitory effect against 4EBP1 and AKT phosphorylation than rapamycin in CRPC cells and prevented the feedback activation of AKT signalling. Importantly, AZD2014 suppressed CRPC cell growth in vitro by suppressing proliferation, apoptosis, cell cycle arrest at G1 phase and autophagy to a greater extent than rapamycin. Moreover, AZD2014 was more efficacious than rapamycin in inhibiting migration, invasion and EMT progression in Doc-sensitive and Doc-resistant CRPC cells. Overall, AZD2014 showed significant antitumour effects. Thereby, the current study highlights a reliable theoretical basis for the clinical application of AZD2014 in both Doc-sensitive and Doc-resistant CRPCs.

Indexed as

ApoptosisAutophagyBenzamidesCell CycleCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationDocetaxelDose-Response Relationship, DrugDrug Resistance, NeoplasmEpithelial-Mesenchymal TransitionHumansImmunophenotypingMaleMechanistic Target of Rapamycin Complex 1BenzamidesDocetaxelMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2MorpholinesProtein Kinase InhibitorsPyrimidinesvistusertibantitumourAZD2014castration-resistant prostate cancerdocetaxelmTORC1 and 2

Identifiers

PMID33507584
PMCPMC7933970
OpenAlexW3122423710

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.