Evidence map›Paper›PMID 15771616›Full record

ReviewCancer science2005

The RET proto-oncogene: a molecular therapeutic target in thyroid cancer.

Yoshinori Kodama, Naoya Asai, Kumi Kawai, Mayumi Jijiwa, Yoshiki Murakumo, Masatoshi Ichihara, Masahide Takahashi

Open access · bronzeAbstract readReview
In one paragraph

Review in Cancer science, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 119 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. AST-487 Inhibits RET Kinase Driven TERT Expression in Bladder Cancer.International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. EVOLUTION OF TARGETED THERAPIES FOR THYROID CARCINOMA.Transactions of the American Clinical and Climatological Association · 2019
    Article
  12. Article
  13. Review
  14. Downregulation of TRIM27 expression inhibits the proliferation of ovarian cancer cells in vitro and in vivo.Laboratory investigation; a journal of technical methods and pathology · 2016
    Article
  15. Article
  16. Overexpression of miR-218 inhibits hepatocellular carcinoma cell growth through RET.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  17. Review
  18. Article
  19. Article
  20. 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 1 institution in 1 country.

Yoshinori KodamaDepartment of Pathology, Center for Neurological Disease and Cancer, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho Showa-ku Nagoya, 466-8550, Japan.
Naoya Asai
Kumi Kawai
Mayumi Jijiwa
Yoshiki Murakumo
Masatoshi Ichihara
Masahide Takahashi
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The RET proto-oncogene is responsible for the development of several human inherited and non-inherited diseases. Germline point mutations were identified in multiple endocrine neoplasia types 2A and 2B, and familial medullary thyroid carcinoma. More than 10 rearranged forms of RET, referred to as RET/PTC 1-9, ELKS/RET and RFP/RET, have been cloned from sporadic and radiation-associated papillary thyroid carcinomas. These mutations induced oncogenic activation of RET tyrosine kinase by different mechanisms. To date, various kinds of therapeutic approaches have been developed for the treatment of RET-associated cancers, including tyrosine kinase inhibitors, gene therapy with dominant negative RET mutants, and RNA interference to abrogate oncogenic mutant RET expression. RET and some signaling molecules that function downstream of RET could be potential targets for the development of selective cancer therapeutics.

Indexed as

RNA InterferenceAntineoplastic AgentsEnzyme InhibitorsGerm-Line MutationHumansNeoplasmsOncogene ProteinsProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene Proteins c-retReceptor Protein-Tyrosine KinasesSignal TransductionAntineoplastic AgentsEnzyme InhibitorsMAS1 protein, humanOncogene ProteinsProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene Proteins c-retReceptor Protein-Tyrosine KinasesRET protein, human

Identifiers

PMID15771616
PMCPMC11159891
OpenAlexW2088699600

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.