Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

ABC gene expression profiles have clinical importance and possibly form a new hallmark of cancer

P. Dvorak, M. Pesta, P. Soucek,

. 2017 ; 39 (5) : 1010428317699800.

Language English Country United States

Document type Journal Article

Grant support
NV15-25618A MZ0 CEP Register

Adenosine triphosphate-binding cassette proteins constitute a large family of active transporters through extracellular and intracellular membranes. Increased drug efflux based on adenosine triphosphate-binding cassette protein activity is related to the development of cancer cell chemoresistance. Several articles have focused on adenosine triphosphate-binding cassette gene expression profiles (signatures), based on the expression of all 49 human adenosine triphosphate-binding cassette genes, in individual tumor types and reported connections to established clinicopathological features. The aim of this study was to test our theory about the existence of adenosine triphosphate-binding cassette gene expression profiles common to multiple types of tumors, which may modify tumor progression and provide clinically relevant information. Such general adenosine triphosphate-binding cassette profiles could constitute a new attribute of carcinogenesis. Our combined cohort consisted of tissues from 151 cancer patients-breast, colorectal, and pancreatic carcinomas. Standard protocols for RNA isolation and quantitative real-time polymerase chain reaction were followed. Gene expression data from individual tumor types as well as a merged tumor dataset were analyzed by bioinformatics tools. Several general adenosine triphosphate-binding cassette profiles, with differences in gene functions, were established and shown to have significant relations to clinicopathological features such as tumor size, histological grade, or clinical stage. Genes ABCC7, A3, A8, A12, and C8 prevailed among the most upregulated or downregulated ones. In conclusion, the results supported our theory about general adenosine triphosphate-binding cassette gene expression profiles and their importance for cancer on clinical as well as research levels. The presence of ABCC7 (official symbol CFTR) among the genes with key roles in the profiles supports the emerging evidence about its crucial role in various cancers. Graphical abstract.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18016627
003      
CZ-PrNML
005      
20201013140900.0
007      
ta
008      
180515s2017 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1177/1010428317699800 $2 doi
035    __
$a (PubMed)28468577
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Dvorak, Pavel $u 1 Department of Biology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
245    10
$a ABC gene expression profiles have clinical importance and possibly form a new hallmark of cancer / $c P. Dvorak, M. Pesta, P. Soucek,
520    9_
$a Adenosine triphosphate-binding cassette proteins constitute a large family of active transporters through extracellular and intracellular membranes. Increased drug efflux based on adenosine triphosphate-binding cassette protein activity is related to the development of cancer cell chemoresistance. Several articles have focused on adenosine triphosphate-binding cassette gene expression profiles (signatures), based on the expression of all 49 human adenosine triphosphate-binding cassette genes, in individual tumor types and reported connections to established clinicopathological features. The aim of this study was to test our theory about the existence of adenosine triphosphate-binding cassette gene expression profiles common to multiple types of tumors, which may modify tumor progression and provide clinically relevant information. Such general adenosine triphosphate-binding cassette profiles could constitute a new attribute of carcinogenesis. Our combined cohort consisted of tissues from 151 cancer patients-breast, colorectal, and pancreatic carcinomas. Standard protocols for RNA isolation and quantitative real-time polymerase chain reaction were followed. Gene expression data from individual tumor types as well as a merged tumor dataset were analyzed by bioinformatics tools. Several general adenosine triphosphate-binding cassette profiles, with differences in gene functions, were established and shown to have significant relations to clinicopathological features such as tumor size, histological grade, or clinical stage. Genes ABCC7, A3, A8, A12, and C8 prevailed among the most upregulated or downregulated ones. In conclusion, the results supported our theory about general adenosine triphosphate-binding cassette gene expression profiles and their importance for cancer on clinical as well as research levels. The presence of ABCC7 (official symbol CFTR) among the genes with key roles in the profiles supports the emerging evidence about its crucial role in various cancers. Graphical abstract.
650    _2
$a ABC transportéry $x biosyntéza $x genetika $7 D018528
650    _2
$a nádory prsu $x genetika $x patologie $7 D001943
650    12
$a karcinogeneze $7 D063646
650    _2
$a kolorektální nádory $x genetika $x patologie $7 D015179
650    _2
$a protein CFTR $x biosyntéza $x genetika $7 D019005
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a regulace genové exprese u nádorů $7 D015972
650    _2
$a lidé $7 D006801
650    _2
$a nádory slinivky břišní $x genetika $x patologie $7 D010190
650    _2
$a receptory sulfonylurey $x biosyntéza $x genetika $7 D064233
650    _2
$a transkriptom $x genetika $7 D059467
655    _2
$a časopisecké články $7 D016428
700    1_
$a Pesta, Martin $u 1 Department of Biology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
700    1_
$a Soucek, Pavel $u 2 Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
773    0_
$w MED00008757 $t Tumour biology the journal of the International Society for Oncodevelopmental Biology and Medicine $x 1423-0380 $g Roč. 39, č. 5 (2017), s. 1010428317699800
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28468577 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180515 $b ABA008
991    __
$a 20201013140857 $b ABA008
999    __
$a ok $b bmc $g 1300251 $s 1013467
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 39 $c 5 $d 1010428317699800 $i 1423-0380 $m Tumor biology $n Tumor Biol $x MED00008757
GRA    __
$a NV15-25618A $p MZ0
LZP    __
$a Pubmed-20180515

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...