Mutation profile variability in the primary tumor and multiple pulmonary metastases of clear cell renal cell carcinoma. A review of the literature and analysis of four metastatic cases
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00669806%3A_____%2F21%3A10434563" target="_blank" >RIV/00669806:_____/21:10434563 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11140/21:10434563 RIV/00216208:11130/21:10434563
Result on the web
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=~a-lkQD7r3" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=~a-lkQD7r3</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/cancers13235906" target="_blank" >10.3390/cancers13235906</a>
Alternative languages
Result language
angličtina
Original language name
Mutation profile variability in the primary tumor and multiple pulmonary metastases of clear cell renal cell carcinoma. A review of the literature and analysis of four metastatic cases
Original language description
(1) Background: There are limited data concerning inter-tumoral and inter-metastatic heterogeneity in clear cell renal cell carcinoma (CCRCC). The aim of our study was to review published data and to examine mutation profile variability in primary and multiple pulmonary metastases (PMs) in our cohort of four patients with metastatic CCRCC. (2) Methods: Four patients were enrolled in this study. The clinical characteristics, types of surgeries, histopathologic results, immunohistochemical and genetic evaluations of corresponding primary tumor and PMs, and follow-up data were recorded. (3) Results: In our series, the most commonly mutated genes were those in the canonically dysregulated VHL pathway, which were detected in both primary tumors and corresponding metastasis. There were genetic profile differences between primary and metastatic tumors, as well as among particular metastases in one patient. (4) Conclusions: CCRCC shows heterogeneity between the primary tumor and its metastasis. Such mutational changes may be responsible for suboptimal treatment outcomes in targeted therapy settings.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30109 - Pathology
Result continuities
Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Cancers
ISSN
2072-6694
e-ISSN
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Volume of the periodical
13
Issue of the periodical within the volume
23
Country of publishing house
CH - SWITZERLAND
Number of pages
13
Pages from-to
5906
UT code for WoS article
000743149800001
EID of the result in the Scopus database
2-s2.0-85119653970