Evidence map›Paper›PMID 23562158›Full record

ArticleCell reports2013

Regulation of telomerase alternative splicing: a target for chemotherapy.

Mandy S Wong, Ling Chen, Christopher Foster, Radhika Kainthla, Jerry W Shay, Woodring E Wright

Abstract read
In one paragraph

Article in Cell reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

  1. XRCC1 is linked to poor prognosis in adenocarcinoma of the esophagogastric junction after radiotherapy: transcriptome and alternative splicing events analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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  15. Diverse regulatory manners of human telomerase reverse transcriptase.Cell communication and signaling : CCS · 2019
    Review
  16. Review
  17. 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

6 authors.

Mandy S WongDepartment of Cell Biology, UT Southwestern Medical Center, Dallas, TX 75390-9039, USA.
Ling Chen
Christopher Foster
Radhika Kainthla
Jerry W Shay
Woodring E Wright

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HEYMACH, JOHN V., MINNA, JOHN D. · 1996 to 2024
$57.4M
Manipulating telomerase alternative splicing for cancer therapyR01CA154805 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI WRIGHT, WOODRING ERIK · 2011 to 2015
$1.6M
Clinical & Basic NIDDK Research Training for Medical StudentsT35DK066141 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI GALINDO, RENE L · 2004 to 2013
$1.0M
NCI NIH HHS CA154805NCI NIH HHS P50 CA070907NCI NIH HHS R01 CA154805NIDDK NIH HHS T-35-DK066141NIDDK NIH HHS T35 DK066141
6 · The paper itself

Abstract

Telomerase is present in human cancer cells but absent in most somatic tissues. The messenger RNA of human telomerase (hTERT) is alternatively spliced into mostly nonfunctional products. We sought to understand splicing so that we could decrease functional splice isoforms to reduce telomerase activity in order to complement direct enzyme inhibition. Unexpectedly, minigenes containing hTERT exons 5-10 flanked by 150-300 bp intronic sequences did not produce alternative splicing. A 1.1 kb region of 38 bp repeats ~2 kb from the exon 6/intron junction restored the exclusion of exons 7 and 8. An element within intron 8, also >1 kb from intron/exon junctions, modulated this effect. Transducing an oligonucleotide complementary to this second element increased nonfunctional hTERT messenger RNA from endogenous telomerase. These results demonstrate the potential of manipulating hTERT splicing for both chemotherapy and regenerative medicine and provide specific sequences deep within introns that regulate alternative splicing in mammalian cells by mechanisms other than the introduction of cryptic splice sites.

Indexed as

Alternative SplicingBase SequenceCell Line, TumorExonsHCT116 CellsHEK293 CellsHeLa CellsHT29 CellsHumansIntronsMolecular Sequence DataOligonucleotides, AntisenseRNA, MessengerTelomeraseOligonucleotides, AntisenseRNA, MessengerTelomerase

Identifiers

PMID23562158
PMCPMC3640656

What OpenQuestion holds

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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.