Evidence map›Paper›PMID 22074739›Full record

ArticleThe American journal of pathology2012

Alterations in nuclear pore architecture allow cancer cell entry into or exit from drug-resistant dormancy.

Yayoi Kinoshita, Tamara Kalir, Jamal Rahaman, Peter Dottino, D Stave Kohtz

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Review
  12. Non-Coding RNAs Are Implicit in Chronic Myeloid Leukemia Therapy Resistance.International journal of molecular sciences · 2022
    Review
  13. Autophagy and Cancer Dormancy.Frontiers in oncology · 2021
    Review
  14. Article
  15. Review
  16. 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

5 authors at 4 institutions in 3 countries.

Yayoi KinoshitaDepartment of Pathology, Mount Sinai School of Medicine, New York, New York 10029, USA.
Tamara Kalir
Jamal Rahaman
Peter Dottino
D Stave Kohtz
Institute of Reproductive Medicine · INAngiologica (Italy) · ITIcahn School of Medicine at Mount Sinai · USVeterinary Oncological Center · IT

Funding

Advanced Microscopy Shared Resource FacilityR24CA095823 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI FRIEDRICH, VICTOR LOUIS · 2002 to 2006
$1.3M
Nuclear Pore Complex Architecture and Drug Resistance in Ovarian CarcinomasR03CA141318 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOHTZ, DONALD STAVE · 2010 to 2011
$167k
CONFOCAL MICROSCOPE FACILITYS10RR009145 · NCRR · MOUNT SINAI SCHOOL OF MEDICINE OF CUNY · PI MASUR, SANDRA K · 1994 to 1994
–
NCI NIH HHS 1R03CA141318NCI NIH HHS 5R24 CA095823-04NCI NIH HHS R03 CA141318NCI NIH HHS R24 CA095823NCRR NIH HHS 1 S10 RR0 9145-01
6 · The paper itself

Abstract

Phenotypic diversity arises in tumors just as it does in developing organisms, and tumor recurrence frequently manifests from the selective survival of divergent drug-resistant cells. Although the expanding tumor cell population may be successfully targeted, drug-resistant cells may persist and sustain the tumor or enter dormancy before igniting a future relapse. Herein, we show that partial knockdown of nucleoporin p62 (NUP62) by small-interfering RNA confers cisplatin resistance to cultured high-grade ovarian carcinoma cells. Treatment with NUP62 small-interfering RNA and cisplatin leaves resistant cells in a state of dormancy; some dormant cells can be induced to proliferate by transient induction of NUP62 expression from an ectopic expression construct. In addition to suggesting functional links between nuclear pore complex architecture and cancer cell survival, the culture system provides a novel experimental window into the dynamics of tumor cell drug resistance and dormancy.

Indexed as

Antineoplastic AgentsCell Cycle CheckpointsCell Line, TumorCell ProliferationCisplatinDrug Resistance, NeoplasmFemaleGene Knockdown TechniquesHumansMembrane GlycoproteinsNeoplasm Recurrence, LocalNuclear PoreNuclear Pore Complex ProteinsOvarian NeoplasmsPhenotypeRNA, Small InterferingAntineoplastic AgentsCisplatinMembrane GlycoproteinsNuclear Pore Complex Proteinsnuclear pore protein p62RNA, Small Interfering

Identifiers

PMID22074739
PMCPMC3338353
OpenAlexW1989193114

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.