• Je něco špatně v tomto záznamu ?

Association between PD-L1 Expression and the Prognosis and Clinicopathologic Features of Non-Clear Cell Renal Cell Carcinoma

M. Chrabańska, N. Szweda-Gandor, M. Rynkiewicz, D. Hraboš, B. Drozdzowska

. 2024 ; 25 (7) : . [pub] 20240331

Jazyk angličtina Země Švýcarsko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc24014520

Grantová podpora
APC Medical University of Silesia

PD-L1 is one of the two programmed cell death 1 (PD-1) ligands and a part of an immune checkpoint system (PD-1/PD-L1) with widespread clinical application. The aim of this study was to investigate PD-L1 expression and its association with clinicopathological and prognostic significance in non-clear cell renal cell carcinoma (non-ccRCC) patients. A total of 41 papillary (pRCC) and 20 chromophobe (chRCC) RCC tumors were examined for PD-L1 expression by immunohistochemistry in the cancer cells and tumor-infiltrating mononuclear cells (TIMCs). PD-L1 positivity was detected in 36.6% pRCC and 85.0% chRCC cancer cells, while PD-L1 positivity was observed in 73.2% pRCC and 50.0% chRCC TIMCs. PD-L1 positivity in both pRCC and chRCC tumor cells was not correlated with any of the examined clinicopathological features, while PD-L1 positivity in TIMCs was associated with the age of patients with pRCC. During follow-up, the death was documented among 6 patients with pRCC. Papillary RCC patients with PD-L1-positive tumor cells were significantly associated with an increased risk of death compared with patients with PD-L1-negative cancer cells. A similar trend was observed when comparing PD-L1 expression in TIMCs. However, no differences in overall survival for PD-L1-positive pRCC patients with compared to PD-L1-negative patients were observed in tumor cells or TIMCs.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc24014520
003      
CZ-PrNML
005      
20240905134132.0
007      
ta
008      
240725s2024 sz f 000 0|eng||
009      
AR
024    7_
$a 10.3390/ijms25073916 $2 doi
035    __
$a (PubMed)38612724
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Chrabańska, Magdalena $u Department of Pathomorphology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland $1 https://orcid.org/0000000177041124
245    10
$a Association between PD-L1 Expression and the Prognosis and Clinicopathologic Features of Non-Clear Cell Renal Cell Carcinoma / $c M. Chrabańska, N. Szweda-Gandor, M. Rynkiewicz, D. Hraboš, B. Drozdzowska
520    9_
$a PD-L1 is one of the two programmed cell death 1 (PD-1) ligands and a part of an immune checkpoint system (PD-1/PD-L1) with widespread clinical application. The aim of this study was to investigate PD-L1 expression and its association with clinicopathological and prognostic significance in non-clear cell renal cell carcinoma (non-ccRCC) patients. A total of 41 papillary (pRCC) and 20 chromophobe (chRCC) RCC tumors were examined for PD-L1 expression by immunohistochemistry in the cancer cells and tumor-infiltrating mononuclear cells (TIMCs). PD-L1 positivity was detected in 36.6% pRCC and 85.0% chRCC cancer cells, while PD-L1 positivity was observed in 73.2% pRCC and 50.0% chRCC TIMCs. PD-L1 positivity in both pRCC and chRCC tumor cells was not correlated with any of the examined clinicopathological features, while PD-L1 positivity in TIMCs was associated with the age of patients with pRCC. During follow-up, the death was documented among 6 patients with pRCC. Papillary RCC patients with PD-L1-positive tumor cells were significantly associated with an increased risk of death compared with patients with PD-L1-negative cancer cells. A similar trend was observed when comparing PD-L1 expression in TIMCs. However, no differences in overall survival for PD-L1-positive pRCC patients with compared to PD-L1-negative patients were observed in tumor cells or TIMCs.
650    _2
$a lidé $7 D006801
650    12
$a karcinom z renálních buněk $x genetika $7 D002292
650    _2
$a antigeny CD274 $x genetika $7 D060890
650    _2
$a antigeny CD279 $7 D061026
650    _2
$a leukocyty $7 D007962
650    _2
$a transkripční faktory $7 D014157
650    12
$a nádory ledvin $x genetika $7 D007680
655    _2
$a časopisecké články $7 D016428
700    1_
$a Szweda-Gandor, Nikola $u Department and Clinic of Internal Medicine, Diabetology and Nephrology, Medical University of Silesia, 40-055 Zabrze, Poland
700    1_
$a Rynkiewicz, Magdalena $u Department of Pathomorphology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland
700    1_
$a Hraboš, Dominik $u Department of Clinical and Molecular Pathology, Faculty of Medicine and Dentistry, Palacky University, 779 00 Olomouc, Czech Republic
700    1_
$a Drozdzowska, Bogna $u Department of Pathomorphology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland $1 https://orcid.org/0000000222876842
773    0_
$w MED00176142 $t International journal of molecular sciences $x 1661-6596 $g Roč. 25, č. 7 (2024)
856    41
$u https://pubmed.ncbi.nlm.nih.gov/38612724 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20240725 $b ABA008
991    __
$a 20240905134126 $b ABA008
999    __
$a ok $b bmc $g 2143964 $s 1226386
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2024 $b 25 $c 7 $e 20240331 $i 1661-6596 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
GRA    __
$a APC $p Medical University of Silesia
LZP    __
$a Pubmed-20240725

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...