Clonal heterogeneity of lymphoid malignancies correlates with poor prognosis. Issue 7 (1st July 2014)

• Record Type: Journal Article
• Authors: Suguro, Miyuki; Yoshida, Noriaki; Umino, Akira; Kato, Harumi; Tagawa, Hiroyuki; Nakagawa, Masao; Fukuhara, Noriko; Karnan, Sivasundaram; Takeuchi, Ichiro; Hocking, Toby D.; Arita, Kotaro; Karube, Kennosuke; Tsuzuki, Shinobu; Nakamura, Shigeo; Kinoshita, Tomohiro; Seto, Masao
• Is Part Of: Cancer science. Volume 105:Issue 7(2014:Jul.)
• Page Start: 897
• Page End: 904
• Publication Date: 2014-07-01
• Subjects: Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.12442
• Languages: English
• ISSNs: 1347-9032

Abstract

<abstract abstract-type="main" id="cas12442-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Clonal heterogeneity in lymphoid malignancies has been recently reported in adult T‐cell lymphoma/leukemia, peripheral T‐cell lymphoma, not otherwise specified, and mantle cell lymphoma. Our analysis was extended to other types of lymphoma including marginal zone lymphoma, follicular lymphoma and diffuse large B‐cell lymphoma. To determine the presence of clonal heterogeneity, 332 cases were examined using array comparative genomic hybridization analysis. Results showed that incidence of clonal heterogeneity varied from 25% to 69% among different types of lymphoma. Survival analysis revealed that mantle cell lymphoma and diffuse large B‐cell lymphoma with clonal heterogeneity showed significantly poorer prognosis, and that clonal heterogeneity was confirmed as an independent predictor of poor prognosis for both types of lymphoma. Interestingly, 8q24.1 (<italic>MYC</italic>) gain, 9p21.3 (<italic>CDKN2A/2B</italic>) loss and 17p13 (<italic>TP53</italic>, <italic>ATP1B2</italic>, <italic>SAT2</italic>, <italic>SHBG</italic>) loss were recurrent genomic lesions among various types of lymphoma with clonal heterogeneity, suggesting at least in part that alterations of these genes may play a role in clonal heterogeneity.</p> </abstract>