Evidence map›Paper›PMID 11455968›Full record

ReviewLeukemia2001

Suppression of apoptosis: role in cell growth and neoplasia.

M K White, J A McCubrey

Abstract readReview
PubMed Publisher
In one paragraph

Review in Leukemia, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 65 citations in OpenAlex.

  1. Nutrition research and practice · 2025
    Article
  2. Kaurene diterpene induces apoptosis in U87 human malignant glioblastoma cells by suppression of anti-apoptotic signals and activation of cysteine proteases.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2013
    Article
  3. Altered mitochondrial apoptotic pathway in placentas from undernourished rat gestations.American journal of physiology. Regulatory, integrative and comparative physiology · 2011
    Article
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  15. Enhanced microtubule-dependent trafficking and p53 nuclear accumulation by suppression of microtubule dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2002
    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

2 authors at 2 institutions in 1 country.

M K WhiteDepartment of Pathology, Anatomy and Cell Biology, The Jefferson Medical College of Thomas Jefferson University, Philadelphia, PA 19107, USA.
J A McCubrey
East Carolina University · USThomas Jefferson University · US

Funding

MECHANISMS OF TRANSFORMATION OF HEMOPOIETIC CELLSR01CA051025 · NCI · EAST CAROLINA UNIVERSITY · PI MC CUBREY, JAMES A · 1992 to 2001
$361k
DIFFERENTIAL REGULATION OF GLUCOSE TRANSPORTER ISOFORMSR29DK045718 · NIDDK · THOMAS JEFFERSON UNIVERSITY · PI WHITE, MARTYN K · 1992 to 1996
–
NCI NIH HHS CA51025NIDDK NIH HHS DK45718
6 · The paper itself

Abstract

A cell is a potentially dangerous thing. In unicellular organisms, cells divide and multiply in a manner that is chiefly determined by the availability of nutritional substrates. In a multicellular organism, each cell has a distinct growth potential that is designed to subsume a role in the function of the whole body. Departure from this path to one of uncontrolled cellular proliferation leads to cancer. For this reason, evolution has endowed cells with an elaborate set of systems that cause errant cells to self-destruct. This process of cell suicide is known as apoptosis or programmed cell death and it plays a crucial role in the growth of both normal and malignant cells. In this review, we describe the mechanisms whereby programmed cell death is induced and executed. In particular, we concentrate on how anti-apoptotic signals generated by cytokines promote cell survival and how these signal transduction pathways may be involved in the pathogenesis of neoplasia. Understanding how these processes contribute to tumorigenesis may suggest new therapeutic options.

Indexed as

ApoptosisAnimalsCaspasesCell DivisionEnzyme ActivationHumansNeoplasmsNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-bcl-2CaspasesNF-kappa BPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-bcl-2

Identifiers

PMID11455968
OpenAlexW2334629408

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.