Evidence map›Paper›PMID 10734317›Full record

ArticleOncogene2000

M6P/IGF2R is mutated in squamous cell carcinoma of the lung.

F M Kong, M S Anscher, M K Washington, J K Killian, R L Jirtle

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.7field-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

35 citing papers in PubMed, 105 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Crosstalk between Calcium and ROS in Pathophysiological Conditions.Oxidative medicine and cellular longevity · 2019
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. WWOX, large common fragile site genes, and cancer.Experimental biology and medicine (Maywood, N.J.) · 2015
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. IGF2R missense single-nucleotide polymorphisms and breast cancer risk: the multiethnic cohort study.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2009
    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

5 authors at 2 institutions in 1 country.

F M KongDepartment of Radiation Oncology, Duke University Medical Center, Durham, North Carolina, NC 27710, USA.
M S Anscher
M K Washington
J K Killian
R L Jirtle
Duke Medical Center · USVanderbilt University Medical Center · US

Funding

TUMOR SUPPRESSOR FUNCTION OF THE M6P/IGF2 RECEPTORR01ES008823 · NIEHS · DUKE UNIVERSITY · PI JIRTLE, RANDY L · 1997 to 2007
$2.2M
SURVIVAL AND CARCINOGENESIS IN TRANSPLANTED HEPATOCYTESR01CA025951 · NCI · DUKE UNIVERSITY · PI JIRTLE, RANDY L · 1985 to 2004
$1.4M
NCI NIH HHS CA25951NIEHS NIH HHS ES08823
6 · The paper itself

Abstract

In addition to the intracellular sorting of lysosomal enzymes, the mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGF2R) plays a critical role in regulating the bioavailability of extracellular proteolytic enzymes and growth factors. It has also been shown to be mutated in a number of human cancers, and to suppress cancer cell growth. The purpose of this study was to determine if the M6P/IGF2R is mutated in lung cancer, a leading cause of cancer death worldwide. Archival pathology specimens were obtained on 22 patients with newly diagnosed, untreated squamous cell carcinoma of the lung. Two polymorphisms in the 3'-untranslated region of the M6P/IGF2R were used to screen lung tumors for loss of heterozygosity (LOH) by PCR amplification of DNA. Nineteen of 22 (86%) patients were informative (heterozygous), and 11/19 (58%) squamous cell carcinomas of the lung had LOH at the M6P/IGF2R locus. The remaining allele in 6/11 (55%) LOH patients contained mutations in either the mannose 6-phosphate or the IGF2 binding domain of the M6P/IGF2R. Thus, the M6P/IGF2R is mutated frequently in squamous cell carcinoma of the lung, providing further support for its function as a tumor suppressor.

Indexed as

MutationAgedAmino Acid SubstitutionBinding SitesCarcinoma, Squamous CellExonsFemaleHeterozygoteHumansLoss of HeterozygosityLung NeoplasmsMaleReceptor, IGF Type 2Receptor, IGF Type 2

Identifiers

PMID10734317
OpenAlexW2106749014

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.