Evidence map›Paper›PMID 32183020›Full record

ReviewInternational journal of molecular sciences2020

The Roles of Cyclin-Dependent Kinases in Cell-Cycle Progression and Therapeutic Strategies in Human Breast Cancer.

Lei Ding, Jiaqi Cao, Wen Lin, Hongjian Chen, Xianhui Xiong, Hongshun Ao, Min Yu, Jie Lin, Qinghua Cui

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 294 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
294citing papers in PubMed, 2 pooled it
34.8field-weighted citation impact, top 1% 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

294 citing papers in PubMed, 2 syntheses or guidelines pooled it, 560 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  12. Phytochemical Profile and Biological Activities ofPharmaceuticals (Basel, Switzerland) · 2026
    Article
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  16. Review
  17. Article
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  19. Observational
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234 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Lei DingLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Jiaqi CaoLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Wen LinLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Hongjian ChenLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Xianhui XiongLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Hongshun AoLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Min YuLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Jie LinLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Qinghua CuiLab of Biochemistry & Molecular Biology, School of Life Sciences, Yunnan University, Kunming 650091, China.
Yunnan University · CN

Funding

National Natural Science Foundation of China 31760331National Natural Science Foundation of China 81360310National Natural Science Foundation of China 81660583National Natural Science Foundation of China 81760507National Natural Science Foundation of China 81860531Yunnan Province Science and Technology Innovation Team No. 2011CI123
6 · The paper itself

Abstract

Cyclin-dependent kinases (CDKs) are serine/threonine kinases whose catalytic activities are regulated by interactions with cyclins and CDK inhibitors (CKIs). CDKs are key regulatory enzymes involved in cell proliferation through regulating cell-cycle checkpoints and transcriptional events in response to extracellular and intracellular signals. Not surprisingly, the dysregulation of CDKs is a hallmark of cancers, and inhibition of specific members is considered an attractive target in cancer therapy. In breast cancer (BC), dual CDK4/6 inhibitors, palbociclib, ribociclib, and abemaciclib, combined with other agents, were approved by the Food and Drug Administration (FDA) recently for the treatment of hormone receptor positive (HR+) advanced or metastatic breast cancer (A/MBC), as well as other sub-types of breast cancer. Furthermore, ongoing studies identified more selective CDK inhibitors as promising clinical targets. In this review, we focus on the roles of CDKs in driving cell-cycle progression, cell-cycle checkpoints, and transcriptional regulation, a highlight of dysregulated CDK activation in BC. We also discuss the most relevant CDK inhibitors currently in clinical BC trials, with special emphasis on CDK4/6 inhibitors used for the treatment of estrogen receptor-positive (ER+)/human epidermal growth factor 2-negative (HER2-) M/ABC patients, as well as more emerging precise therapeutic strategies, such as combination therapies and microRNA (miRNA) therapy.

Indexed as

Cell CycleAntineoplastic AgentsBreast NeoplasmsClinical Trials as TopicCyclin-Dependent KinasesFemaleGene Expression Regulation, NeoplasticHumansProtein Kinase InhibitorsAntineoplastic AgentsCyclin-Dependent KinasesProtein Kinase Inhibitorsbreast cancer (BC)CDK inhibitorcell cycleclinic therapycyclin-dependent kinase (CDK)

Identifiers

PMID32183020
PMCPMC7139603
OpenAlexW3010714596

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.