Evidence map›Paper›PMID 33891890›Full record

ReviewCancer cell2021

Targeting cell-cycle machinery in cancer.

Jan M Suski, Marcin Braun, Vladislav Strmiska, Piotr Sicinski

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 326 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
326citing papers in PubMed, 1 pooled it
57.1field-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

326 citing papers in PubMed, 1 synthesis or guideline pooled it, 556 citations in OpenAlex.

  1. Pooled it
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  7. Characterization of immune landscape and prognostic value of IL-17-related signature in uterine corpus endometrial carcinoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
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  10. Review
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266 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

4 authors at 1 institution in 2 countries.

Jan M SuskiDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA.
Marcin BraunDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA; Department of Pathology, Chair of Oncology, Medical University of Lodz, 92-213 Lodz, Poland.
Vladislav StrmiskaDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA.
Piotr SicinskiDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02215, USA; Department of Genetics, Blavatnik Institute, Harvard Medical School, Boston, MA 02115, USA. Electronic address: peter_sicinski@dfci.harvard.edu.
Harvard University · US

Funding

Tissue and Pathology CoreP50CA168504 · NCI · DANA-FARBER CANCER INST · PI LEIF W ELLISEN, NANCY U LIN · 2013 to 2026
$30.1M
Novel therapeutic approaches with CDK4/6 inhibitors for melanoma treatmentR01CA236226 · NCI · DANA-FARBER CANCER INST · PI SICINSKI, PETER · 2019 to 2023
$2.4M
CDC7 kinase in normal and cancer cells: potential implications for cancer treatmentR01CA247375 · NCI · DANA-FARBER CANCER INST · PI SICINSKI, PETER · 2020 to 2024
$2.3M
Novel functions of D-type and E-type cyclins in normal and in cancer cellsR01CA202634 · NCI · DANA-FARBER CANCER INST · PI SICINSKI, PETER · 2016 to 2020
$2.1M
NCI NIH HHS P50 CA168504NCI NIH HHS R01 CA202634NCI NIH HHS R01 CA236226NCI NIH HHS R01 CA247375
6 · The paper itself

Abstract

Abnormal activity of the core cell-cycle machinery is seen in essentially all tumor types and represents a driving force of tumorigenesis. Recent studies revealed that cell-cycle proteins regulate a wide range of cellular functions, in addition to promoting cell division. With the clinical success of CDK4/6 inhibitors, it is becoming increasingly clear that targeting individual cell-cycle components may represent an effective anti-cancer strategy. Here, we discuss the potential of inhibiting different cell-cycle proteins for cancer therapy.

Indexed as

AnimalsAntineoplastic AgentsCell CycleCyclin DCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin EHumansMiceMolecular Targeted TherapyNeoplasmsAntineoplastic AgentsCDK4 protein, humanCDK6 protein, humanCyclin DCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin E

Identifiers

PMID33891890
PMCPMC8206013
OpenAlexW3156721991

What OpenQuestion holds

Textmetadata
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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.