Evidence map›Paper›PMID 30987032›Full record

ArticlePharmaceuticals (Basel, Switzerland)2019

CDK11 Loss Induces Cell Cycle Dysfunction and Death of BRAF and NRAS Melanoma Cells.

Rehana L Ahmed, Daniel P Shaughnessy, Todd P Knutson, Rachel I Vogel, Khalil Ahmed, Betsy T Kren, Janeen H Trembley

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. SCFEMBO reports · 2022
    Article
  7. Article
  8. Novel insights into the pathogenesis and treatment of NRAS mutant melanoma.Expert review of precision medicine and drug development · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Article
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

7 authors at 2 institutions in 1 country.

Rehana L AhmedDepartment of Dermatology, University of Minnesota, Minneapolis, MN 55455, USA. ahme0056@umn.edu.
Daniel P ShaughnessyResearch Service, Minneapolis VA Health Care System, Minneapolis, MN 55417, USA. shaug028@umn.edu.
Todd P KnutsonDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA. knut0297@umn.edu.
Rachel I VogelMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA. isak0023@umn.edu.
Khalil AhmedMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA. krenx@umn.edu.
Betsy T KrenMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA. trem0005@umn.edu.
Janeen H TrembleyMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA. trem0005@umn.edu.
University of Minnesota · USMinneapolis VA Health Care System · US

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
Mechanisms of CK2-regulated prostate cancer survival and deathI01BX003282 · VA · MINNEAPOLIS VA MEDICAL CENTER · PI AHMED, KHALIL · 2016 to 2019
–
BLRD VA I01 BX003282NCATS NIH HHS UL1 TR002494Randy Shaver Cancer Research and Community Fund N/AU.S. Department of Veterans Affairs BX003282
6 · The paper itself

Abstract

Cyclin dependent kinase 11 (CDK11) is a protein kinase that regulates RNA transcription, pre-mRNA splicing, mitosis, and cell death. Targeting of CDK11 expression levels is effective in the experimental treatment of breast and other cancers, but these data are lacking in melanoma. To understand CDK11 function in melanoma, we evaluated protein and RNA levels of CDK11, Cyclin L1 and Cyclin L2 in benign melanocytes and BRAF- as well as NRAS-mutant melanoma cell lines. We investigated the effectiveness of reducing expression of this survival kinase using RNA interference on viability, clonal survival, and tumorsphere formation in melanoma cell lines. We examined the impact of CDK11 loss in BRAF-mutant melanoma on more than 700 genes important in cancer signaling pathways. Follow-up analysis evaluated how CDK11 loss alters cell cycle function in BRAF- and NRAS-mutant melanoma cells. We present data on CDK11, CCNL1 and CCNL2 mRNA expression in melanoma patients, including prognosis for survival. In sum, we found that CDK11 is necessary for melanoma cell survival, and a major impact of CDK11 loss in melanoma is to cause disruption of the cell cycle distribution with accumulation of G1- and loss of G2/M-phase cancer cells.

Indexed as

cancerCDK11cell cycleCyclin L1Cyclin L2melanoma

Identifiers

PMID30987032
PMCPMC6631185
OpenAlexW2929459150

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.