Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Translocation t(11;14)(q13;q32) in chronic lymphoid disorders.

V Brito-Babapulle1, J Ellis, E Matutes

  • 1Academic Department of Haematology, Institute of Cancer Research, London, United Kingdom.

Genes, Chromosomes & Cancer
|September 1, 1992
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia.

Nature genetics·1997
Same author

The human T-cell lymphotropic viruses types I/II are not involved in T prolymphocytic leukemia and large granular lymphocytic leukemia.

Leukemia·1997
Same author

The significance of minimal residual disease in hairy cell leukaemia treated with deoxycoformycin: a long-term follow-up study.

British journal of haematology·1997
Same author

G-CSF mobilization of haemopoietic cell populations in SCID mice engrafted with human leukaemia.

Bone marrow transplantation·1997
Same author

Sezary cell leukaemia: a distinct T cell disorder or a variant form of T prolymphocytic leukaemia?

Leukemia·1997
Same author

Treatment of T-cell prolymphocytic leukemia with human CD52 antibody.

Journal of clinical oncology : official journal of the American Society of Clinical Oncology·1997

The t(11;14) chromosomal translocation is linked to mature B-cell leukemias, particularly those with lymphoplasmacytic features. This finding aids in classifying B-cell disorders more precisely.

Area of Science:

  • Hematology
  • Oncology
  • Cytogenetics

Background:

  • The t(11;14)(q13;q32) translocation involves the BCL1 oncogene and is associated with B-lymphoproliferative disorders.
  • This abnormality may define specific lymphoma subtypes, necessitating reevaluation of its significance in B-cell malignancies.
  • Objective classification using morphology, histology, and immunophenotype is crucial for understanding B-cell disorders.

Purpose of the Study:

  • To reexamine the significance of the t(11;14) translocation in B-cell disorders.
  • To correlate the t(11;14) abnormality with specific subtypes of B-cell leukemias.
  • To assess the utility of morphology and immunophenotype in conjunction with cytogenetics for disease classification.

Main Methods:

  • Analysis of 90 patients with chronic lymphoid disorders exhibiting clonal chromosome abnormalities.

Related Experiment Videos

  • Detailed cytogenetic analysis to detect the t(11;14)(q13;q32) translocation.
  • Morphological and immunophenotypic assessment of leukemic cells.
  • Main Results:

    • The t(11;14) translocation was identified in 16 out of 90 patients.
    • The translocation was present in leukemic B-cell disorders including B-prolymphocytic leukemia, chronic lymphocytic leukemia with prolymphocytes, intermediate non-Hodgkin lymphoma, lymphoplasmacytic lymphoma, and splenic lymphoma with villous lymphocytes.
    • Notably, t(11;14) was absent in chronic lymphocytic leukemia and hairy cell leukemia.
    • Morphological and immunophenotypic analysis indicated lymphoplasmacytic features in cases with t(11;14).

    Conclusions:

    • The t(11;14) translocation is a recurrent abnormality in leukemias of mature B cells.
    • This translocation is particularly associated with B-cell leukemias exhibiting lymphoplasmacytic differentiation.
    • Cytogenetic findings combined with morphology and immunophenotype enhance the classification of B-cell lymphoproliferative disorders.