Cited by 129

The DOI matches its Crossref record.

A novel K509I mutation of KIT identified in familial mastocytosis‐in vitro and in vivo responsiveness to imatinib therapy

Zhang, Ling Yan, Smith, Matthew L., Schultheis, Beate, Fitzgibbon, Jude, Lister, T. Andrew, Melo, Junia V., Cross, Nicholas C.P., Cavenagh, Jamie D.·2006·Leukemia Research

Abstract

KIT mutation has been implicated in sporadic mastocytosis, yet clusters in only a few sites in the molecule. For those malignancies associated with KIT mutation or over-expression, imatinib offers a specific therapeutic option, yet it has no effect on D816V mutation commonly seen in sporadic mastocytosis. The majority of cases of familial mastocytosis seem to lack KIT mutation. We report a kindred with mastocytosis in whom in vitro and in vivo sensitivity to imatinib was demonstrated. Mutation analysis of the KIT coding region in this family identified a novel A>T mutation at nucleotide 1547 [K509I] in exon 9 in both of the affected patients.

Overview

Integrity signals

Registry

Crossref · 10.1016/j.leukres.2005.08.015

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

No references could be resolved yet.

Research works printed but not linked: 25

  1. Scheijen, 2002, Tyrosine kinase oncogenes in normal hematopoiesis and hematological disease, Oncogene, 21, 3314, 10.1038/sj.onc.1205317 · DOI
  2. Tsujimura, 1996, Constitutive activation of c-kit in FMA3 murine mastocytoma cells caused by deletion of seven amino acids at the juxtamembrane domain, Blood, 87, 273, 10.1182/blood.V87.1.273.273 · DOI
  3. Furitsu, 1993, Identification of mutations in the coding sequence of the proto-oncogene c-kit in a human mast cell leukemia cell line causing ligand-independent activation of c-kit product, J Clin Invest, 92, 1736, 10.1172/JCI116761 · DOI
  4. Buttner, 1998, Identification of activating c-kit mutations in adult-, but not in childhood-onset indolent mastocytosis: a possible explanation for divergent clinical behavior, J Invest Dermatol, 111, 1227, 10.1046/j.1523-1747.1998.00414.x · DOI
  5. Ning, 2001, Signal transducer and activator of transcription 3 activation is required for Asp(816) mutant c-Kit-mediated cytokine-independent survival and proliferation in human leukemia cells, Blood, 97, 3559, 10.1182/blood.V97.11.3559 · DOI
  6. Zermati, 2003, Effect of tyrosine kinase inhibitor STI571 on the kinase activity of wild-type and various mutated c-kit receptors found in mast cell neoplasms, Oncogene, 22, 660, 10.1038/sj.onc.1206120 · DOI
  7. Pardanani, 2003, Imatinib for systemic mast-cell disease, Lancet, 362, 535, 10.1016/S0140-6736(03)14115-3 · DOI
  8. Pardanani, 2004, FIP1L1-PDGFRA fusion: prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia, Blood, 104, 3038, 10.1182/blood-2004-03-0787 · DOI
  9. Akin, 2003, A novel form of mastocytosis associated with a transmembrane c-Kit mutation and response to imatinib, Blood, 103, 3222, 10.1182/blood-2003-11-3816 · DOI · Paper page
  10. Valent, 2001, Diagnostic criteria and classification of mastocytosis: a consensus proposal, Leuk Res, 25, 603, 10.1016/S0145-2126(01)00038-8 · DOI
  11. Cross, 1994, An optimized multiplex polymerase chain reaction (PCR) for detection of BCR-ABL fusion mRNAs in haematological disorders, Leukemia, 8, 186
  12. Ye, 2001, An efficient procedure for genotyping single nucleotide polymorphisms, Nucleic Acids Res, 29, E88, 10.1093/nar/29.17.e88 · DOI
  13. Caruana, 1999, Isoforms of c-KIT differ in activation of signalling pathways and transformation of NIH3T3 fibroblasts, Oncogene, 18, 5573, 10.1038/sj.onc.1202939 · DOI
  14. Voytyuk, 2003, Src family kinases are involved in the differential signaling from two splice forms of c-Kit, J Biol Chem, 278, 9159, 10.1074/jbc.M211726200 · DOI
  15. Clark, 1990, Familial urticaria pigmentosa, Arch Intern Med, 150, 1742, 10.1001/archinte.150.8.1742 · DOI
  16. Fowler, 1986, Familial urticaria pigmentosa, Arch Dermatol, 122, 80, 10.1001/archderm.122.1.80 · DOI
  17. Hartmann, 2001, Mastocytosis: recent advances in defining the disease, Br J Dermatol, 144, 682, 10.1046/j.1365-2133.2001.04123.x · DOI
  18. Longley, 1999, Activating and dominant inactivating c-KIT catalytic domain mutations in distinct clinical forms of human mastocytosis, Proc Natl Acad Sci USA, 96, 1609, 10.1073/pnas.96.4.1609 · DOI
  19. Rosbotham, 1999, Lack of c-kit mutation in familial urticaria pigmentosa, Br J Dermatol, 140, 849, 10.1046/j.1365-2133.1999.02814.x · DOI
  20. Sato-Matsumura, 1999, Analysis of c-kit exon 11 and exon 17 of urticaria pigmentosa that occurred in monozygotic twin sisters, Br J Dermatol, 140, 1130, 10.1046/j.1365-2133.1999.02890.x · DOI
  21. Tang, 2004, A germline mutation in KIT in familial diffuse cutaneous mastocytosis, J Med Genet, 41, e88, 10.1136/jmg.2003.015156 · DOI · Paper page
  22. Nishida, 1998, Familial gastrointestinal stromal tumours with germline mutation of the KIT gene, Nat Genet, 19, 323, 10.1038/1209 · DOI
  23. Beghini, 2001, Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa, Cancer, 92, 657, 10.1002/1097-0142(20010801)92:3<657::AID-CNCR1367>3.0.CO;2-D · DOI
  24. Carballo, 2005, Novel c-KIT germline mutation in a family with gastrointestinal stromal tumors and cutaneous hyperpigmentation, Am J Med Genet A, 132, 361, 10.1002/ajmg.a.30388 · DOI
  25. Marshall, 1990, Achalasia due to diffuse esophageal leiomyomatosis and inherited as an autosomal dominant disorder. Report of a family study, Gastroenterology, 98, 1358, 10.1016/0016-5085(90)90357-7 · DOI

Cited by

Sorted by citations

See all 129

Metadata

Authors
Zhang, L. Y., Smith, M. L., Schultheis, B., Fitzgibbon, J., Lister, T. A., Melo, J. V., Cross, N. C. P., & Cavenagh, J. D.
Venue
Leukemia Research
Publisher
Elsevier BV
Published
2006-04
Volume
30
Issue
4
Pages
373-378
ISSN
0145-2126
Cited by
129
References
0
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: A novel K509I mutation of KIT identified in familial mastocytosis‐in vitro and in vivo responsiveness to imatinib therapy. https://app.cochat.ai/papers/10.1016/j.leukres.2005.08.015
The paper
Zhang, L. Y., Smith, M. L., Schultheis, B., Fitzgibbon, J., Lister, T. A., Melo, J. V., Cross, N. C. P., & Cavenagh, J. D. (2006). A novel K509I mutation of KIT identified in familial mastocytosis‐in vitro and in vivo responsiveness to imatinib therapy. Leukemia Research. https://doi.org/10.1016/j.leukres.2005.08.015