Evidence map›Paper›PMID 16847266›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2006

Genes and pathways downstream of telomerase in melanoma metastasis.

Sepideh Bagheri, Mehdi Nosrati, Shang Li, Sylvia Fong, Sima Torabian, Javier Rangel, Dan H Moore, Scot Federman, Rebecca R Laposa, Frederick L Baehner and 6 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 131 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Telomere Length: A Cardiovascular Biomarker and a Novel Therapeutic Target.International journal of molecular sciences · 2022
    Review
  5. Review
  6. Article
  7. The Role of Telomerase in Breast Cancer's Response to Therapy.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Telomerase Reverse Transcriptase and p53 Regulate Mammalian Peripheral Nervous System and CNS Axon Regeneration Downstream of c-Myc.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  14. Review
  15. 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

16 authors at 5 institutions in 1 country.

Sepideh BagheriAuerback Melanoma Research Laboratory, Cutaneous Oncology Program, Comprehensive Cancer Center, University of California, San Francisco, CA 94115, USA.
Mehdi Nosrati
Shang Li
Sylvia Fong
Sima Torabian
Javier Rangel
Dan H Moore
Scot Federman
Rebecca R Laposa
Frederick L Baehner
Richard W Sagebiel
James E Cleaver
Christopher Haqq
Robert J Debs
Elizabeth H Blackburn
Mohammed Kashani-Sabet
University of California, San Francisco · USDana-Farber Cancer Institute · USCalifornia Pacific Medical Center · USNorthern California Melanoma Center · USUCSF Helen Diller Family Comprehensive Cancer Center · US

Funding

Synergism of telomere maintenance and telomerase with cancer-promoting signalingR01CA096840 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLACKBURN, ELIZABETH H · 2002 to 2016
$4.8M
Validation of Genomic Targets in MelanomaR01CA114337 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KASHANI-SABET, MOHAMMED · 2005 to 2015
$3.2M
Identifying Genes that Cause Lung Cancer to ProgressR01CA096666 · NCI · CALIFORNIA PACIFIC MED CTR RES INSTITUTE · PI DEBS, ROBERT J · 2003 to 2006
$1.7M
Non-viral Cutaneous Gene DeliveryR03AR049378 · NIAMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KASHANI-SABET, MOHAMMED · 2003 to 2005
$227k
NCI NIH HHS CA114337NCI NIH HHS CA96666NCI NIH HHS CA96840NCI NIH HHS R01 CA096666NCI NIH HHS R01 CA096840NCI NIH HHS R01 CA114337NIAMS NIH HHS R03 AR049378
6 · The paper itself

Abstract

Recent studies have demonstrated a role for telomerase in driving tumor progression, but its mechanism of action remains unclear. Here we show that stable, ribozyme-mediated suppression of mouse telomerase RNA reduced telomerase RNA expression, telomerase activity, and telomere length, which significantly reduced tumor invasion and metastatic potential. Our studies reveal that previously unidentified effects of telomerase may mediate its tumor-promoting effects. First, reducing telomerase activity induced a more dendritic morphology, accompanied by increased melanin content and increased expression of tyrosinase, a key enzyme in melanin biosynthesis. Second, gene expression profiling revealed that telomerase targeting down-regulated expression of several glycolytic pathway genes, with a corresponding decrease in glucose consumption and lactate production. Thus, telomerase activity controls the glycolytic pathway, potentially altering the energy state of tumor cells and thereby modulating tyrosinase activity and melanin production. These studies have important implications for understanding the mechanisms by which telomerase promotes tumor invasion and metastasis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell DifferentiationGene Expression ProfilingGlucoseLactatesMelaninsMelanomaMelanoma, ExperimentalMiceMice, Inbred C57BLMonophenol MonooxygenaseNeoplasm InvasivenessNeoplasm MetastasisTelomeraseGlucoseLactatesMelaninsMonophenol MonooxygenaseTelomerase

Identifiers

PMID16847266
PMCPMC1544082
OpenAlexW1969066171

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.