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Copyright ©2014 Baishideng Publishing Group Co.
World J Gastroenterol. Apr 14, 2014; 20(14): 3778-3794
Published online Apr 14, 2014. doi: 10.3748/wjg.v20.i14.3778
Table 2 Summary of human leukocyte antigen-G evaluations in colorectal cancer and related colonic diseases of the gastrointestinal tract
Sample typeHLA-GsMethodsDisease, nRelevancesRef.
Tumor DNAHLA-GRT-PCRCRC, n = 39HLA-G mRNA was significantly more expressed in CRC (87.2%) than in the extra neoplastic tissue[24]
Tumor tissueHLA-GIHCCRC, n = 201HLA-G is over-expressed in primary CRC sites (64.6%), but not in the normal CRC tissues or benign adenomas[25]
Tumor tissueHLA-GIHCUC, n = 24; CD, n = 19HLA-G and IL-10 are highly expressed in UC but not in CD tissue biopsies[154]
Tumor tissueHLA-GIHCCRC, n = 60; DA, n = 67; BC, n = 37; AC, n = 52HLA-G is over-expressed in 52 % of CRC lesions and also in 79% of PDAs, 76% in BC and 75% AC[26]
Tumor tissueHLA-GIHCCRC, n = 415HLA-G is expressed in > 30% of CRC lesions (data summarize published data collected until 2008)[16]
Tumor tissueHLA-GIHCCRC, n = 154HLA-G is expressed in > 30% of CRC lesions (data summarize published data collected until 2005)[17]
SerumsHLA-GELISACRC, n = 144Higher sHLA-G levels in CRC (median 124.3 U/mL) compared to benign colorectal diseases (cut off value 88.6 U/mL). CEA showed less sensitivity e specificity[27]
PlasmasHLA-GELISACRC, n = 37sHLA-G as a diagnostic biomarker for the detection of early CRC (median 84 U/mL) with respect to BD (median 34 U/mL)[28]
PBMCsHLA-GELISAHD, n = 30; CD, n = 10; UC, n = 18Spontaneous secretion of sHLA-G from cultured PBMCs of CD but not in UC and BD[161]
Secretion of sHLA-G in CD patient cultures and BD but no in UC, after LPS stimulation
Plasma and PBMCHLA-GELISAUC, n = 27; CD, n = 22Immunosuppressive therapy decreases sHLA-G hyperproduction in CD and induces its release in UD, in both plasma and in PBMC culture supernatants[162]