Downregulation of ABCD1 in Human Renal Cell Carcinoma

2009 ◽  
Vol 24 (3) ◽  
pp. 171-178 ◽  
Author(s):  
Tzyh-Chyuan Hour ◽  
Yi-Zih Kuo ◽  
Guang-Yaw Liu ◽  
Wang-Yi Kang ◽  
Chao-Yuan Huang ◽  
...  

Renal cell carcinoma (RCC) is the most common malignant tumor of the kidney. Delayed diagnosis may result in progression and metastasis. Markers for early detection of RCC are lacking. The ATP-binding cassette transporter D1 (ABCD1) is located in the human peroxisome membrane. Its mutation causes X-linked adrenoleukodystrophy (X-ALD), a peroxisomal disorder affecting lipid storage. The role of ABCD1 in human renal tumorigenesis was unclear. In this study, three pairs of RCC tissues were examined by cDNA microarray and data suggested that ABCD1 mRNA is downregulated. Downregulation of ABCD1 expression was confirmed by real-time PCR. ABCD1 expression was also downregulated in four renal cancer cell lines compared to immortalized benign renal tubular cells. ABCD1 mRNA and protein expression levels assessed by immunohistochemistry in the RCC tissues were similar between genders, tumor grades, and tumor stages. Immunohisto-chemical assays also showed that ABCD1 expression was significantly higher in normal than in cancerous tissues (p<0.001). ABCD1 downregulation may be involved in human renal tumorigenesis.

2020 ◽  
Vol 10 (2) ◽  
pp. 195-202
Author(s):  
Yunxing Liu

To select human renal cell carcinoma cell lines VMRC-RCZ After resuscitation, culture and passage, the cell concentration was adjusted to 1 × 106/ml, and the experiment was divided into a control group, a renal cancer cell + DC group (DC group), and a renal cancer cell + DC+ hTERTtransfection group (transfection Group), a total of 3 groups; the recombinant eukaryotic expression plasmid hTERT-IRES2-EGFP was constructed and transfected into mature DC; the renal cancer cell + DC group was transfected with the empty plasmid, and the renal cancer cell + DC+ hTERT transfection group was transfected with the overexpression plasmid The transfection efficiency was detected by RT-PCR method. Cultured for 12 h and 24 h respectively, the percentage of HLA-DR, CD40 and MHC-II molecules in three groups of DC immunophenotypes was determined according to flow cytometry assay, and the cytokines IL-12 and TNF-α expression level, DC apoptosis rate was detected by in situ hybridization, the rate of tumor cell proliferation was measured according to MTT method, and cell cycle was determined through flow cytometry.


2000 ◽  
Vol 28 (6) ◽  
pp. 383-390 ◽  
Author(s):  
C. Fleck ◽  
B. Bachner ◽  
S. Göckeritz ◽  
E. Karge ◽  
U. Strohm ◽  
...  

1996 ◽  
Vol 3 (5) ◽  
pp. 392-396 ◽  
Author(s):  
Teiichiro Aoyagi ◽  
Kunio Takishima ◽  
Masamichi Hayakawa ◽  
Hiroshi Nakamura

2004 ◽  
Vol 171 (4S) ◽  
pp. 266-267
Author(s):  
Sean McLaughlin ◽  
Eric Wallen ◽  
William K. Funkhouser ◽  
Raj S. Pruthi

2010 ◽  
Vol 183 (4S) ◽  
Author(s):  
Jeong Seok Hwa ◽  
Fernando J. Kim ◽  
Binod Kumar ◽  
Sweaty Koul ◽  
Randall Meacham ◽  
...  

2017 ◽  
Vol 10 (2) ◽  
pp. 142-152 ◽  
Author(s):  
Junichiro Miyazaki ◽  
Keiichi Ito ◽  
Tomonobu Fujita ◽  
Yuriko Matsuzaki ◽  
Takako Asano ◽  
...  

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