Evidence map›Paper›PMID 25747534›Full record

ReviewThe American journal of pathology2015

Cyclin-dependent kinase inhibitors and the treatment of gastrointestinal cancers.

Sameh Mikhail, Christopher Albanese, Michael J Pishvaian

Open access · bronzeAbstract readReview
In one paragraph

Review in The American journal of pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 32 citations in OpenAlex.

  1. CDK2-Mediated Phosphorylation ofResearch (Washington, D.C.) · 2026
    Article
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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

3 authors at 3 institutions in 1 country.

Sameh MikhailJames Cancer Hospital and Solove Research Institute, The Ohio State University Comprehensive Cancer Center, Columbus, Ohio.
Christopher AlbaneseLombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia; Department of Pathology, Georgetown University Medical Center, Washington, District of Columbia. Electronic address: albanese@georgetown.edu.
Michael J PishvaianLombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, District of Columbia.
Georgetown University · USGeorgetown University Medical Center · USThe Ohio State University · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Culturing viably captured circulating tumor cells using conditional reprogrammingR21CA182050 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI COTE, RICHARD JAMES · 2014 to 2015
$381k
NCI NIH HHS P30 CA051008NCI NIH HHS P30 CA51008-18NCI NIH HHS R21 CA182050
6 · The paper itself

Abstract

The cell cycle is a highly conserved and tightly regulated biological system that controls cellular proliferation and differentiation. The cell cycle regulatory proteins, which include the cyclins, the cyclin-dependent kinases (CDKs), and the CDK inhibitors, are critical for the proper temporal and spatial regulation of cellular proliferation. Conversely, alterations in cell cycle regulatory proteins, leading to the loss of normal cell-cycle control, are a hallmark of many cancers, including gastrointestinal cancers. Accordingly, overexpression of CDKs and cyclins and by contrast loss of CDK inhibitors, are all linked to gastrointestinal cancers and are often associated with less favorable prognoses and outcomes. Because of the importance that the cell cycle regulatory proteins play in tumorigenesis, currently there is a broad spectrum of cell-cycle inhibitors under development that, as a group, hold promise as effective cancer treatments. In support of this approach to cancer treatment, the growing availability of molecular diagnostics techniques may help in identifying patients who have driving abnormalities in the cell-cycle machinery and are thus more likely to respond to cell-cycle inhibitors. In this review, we discuss the prevalence of cell-cycle abnormalities in patients with gastrointestinal cancers and provide a preclinical and clinical overview of new agents that target cell-cycle abnormalities with a special emphasis on gastrointestinal cancers.

Indexed as

AnimalsAntineoplastic AgentsCell CycleCell Transformation, NeoplasticCyclin-Dependent KinasesHumansProtein Kinase InhibitorsStomach NeoplasmsAntineoplastic AgentsCyclin-Dependent KinasesProtein Kinase Inhibitors

Identifiers

PMID25747534
PMCPMC5707194
OpenAlexW2117941491

What OpenQuestion holds

Textmetadata
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.