Genomewide profiling of copy-number alteration in monoclonal gammopathy of undetermined significance

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F16%3A00075965" target="_blank" >RIV/65269705:_____/16:00075965 - isvavai.cz</a>

Alternative codes found

RIV/00216224:14310/16:00088878 RIV/61988987:17110/16:A1701LZK RIV/00843989:_____/16:E0105649 RIV/00064173:_____/16:N0000225

Result on the web

<a href="https://onlinelibrary.wiley.com/doi/epdf/10.1111/ejh.12774" target="_blank" >https://onlinelibrary.wiley.com/doi/epdf/10.1111/ejh.12774</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1111/ejh.12774" target="_blank" >10.1111/ejh.12774</a>

Result language

angličtina

Original language name

Genomewide profiling of copy-number alteration in monoclonal gammopathy of undetermined significance

Original language description

Monoclonal gammopathy of undetermined significance (MGUS) is a benign condition with an approximate 1% annual risk of symptomatic plasma cell disorder development, mostly to multiple myeloma (MM). We performed genomewide screening of copy-number alterations (CNAs) in 90 MGUS and 33 MM patients using high-density DNA microarrays. We identified CNAs in a smaller proportion of MGUS (65.6%) than in MM (100.0%, P = 1.31 x 10(-5)) and showed median number of CNAs is lower in MGUS (3, range 0-22) than in MM (13, range 4-38, P = 1.82 x 10(-10)). In the MGUS cohort, the most frequent losses were located at 1p (5.6%), 6q (6.7%), 13q (30.0%), 14q (14.4%), 16q (8.9%), 21q (5.6%), and gains at 1q (23.3%), 2p (6.7%), 6p (13.3%), and Xq (7.8%). Hyperdiploidy was detected in 38.9% of MGUS cases, and the most frequent whole chromosome gains were 3 (25.6%), 5 (23.3%), 9 (37.8%), 15 (23.3%), and 19 (32.2%). We also identified CNAs such as 1p, 6q, 8p, 12p, 13q, 16q losses, 1q gain and hypodiploidy, which are potentially associated with an adverse prognosis in MGUS. In summary, we showed that MGUS is similar to MM in that it is a genetically heterogeneous disorder, but overall cytogenetic instability is lower than in MM, which confirms that genetic abnormalities play important role in monoclonal gammopathies.

Czech name

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Czech description

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Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

—

OECD FORD branch

30200 - Clinical medicine

Project

<a href="/en/project/NT13492" target="_blank" >NT13492: Role of genetic abnormalities in development and progression of precancerosis monoclonal gammopathy of undetermined significance</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2016

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

European Journal of Haematology

ISSN

0902-4441

e-ISSN

—

Volume of the periodical

97

Issue of the periodical within the volume

6

Country of publishing house

US - UNITED STATES

Number of pages

8

Pages from-to

568-575

UT code for WoS article

000388632400010

EID of the result in the Scopus database

2-s2.0-84994365848