## Abstract Primary effusion lymphoma (PEL) is a large B‐cell neoplasm with an unfavorable prognosis and limited therapeutic options. In this study, cancer testis antigens (CTA) were investigated as potential immunotherapeutic targets in patients with PEL. Baseline expression of a panel of 11 CTA w
Cancer testis antigens in human melanoma stem cells: Expression, distribution, and methylation status
✍ Scribed by Luca Sigalotti; Alessia Covre; Susan Zabierowski; Benjamin Himes; Francesca Colizzi; Pier Giorgio Natali; Meenhard Herlyn; Michele Maio
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 157 KB
- Volume
- 215
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Neoplastic populations with stem cell potential have been most recently identified in human cutaneous melanoma, and initially characterized for their phenotypic profile. Being melanoma stem cells (MSC) the most desirable target of therapeutic intervention, we asked whether they express the epigenetically‐regulated cancer testis antigens (CTA) on which melanoma immunotherapy is increasingly focusing. Reverse transcription‐PCR analyses identified the presence of the large majority of investigated CTA (i.e., MAGE, GAGE, NY‐ESO, and SSX families) in different MSC populations. MSC expressed MAGE‐A proteins as detected by western blot; noteworthy, the distribution of MAGE‐A proteins was highly homogeneous within given MSC populations as shown by confocal immunofluorescence. Promoter methylation studies unveiled a homogeneously‐demethylated MAGE‐A3 promoter that paired MAGE‐A3 expression in MSC. Altogether these findings demonstrate that MSC can be efficiently targeted by CTA‐directed immunotherapeutic approaches, and suggest that epigenetic patterns most likely drive the expression of CTA in MSC as previously shown for melanoma cells. J. Cell. Physiol. 215: 287–291, 2008. © 2008 Wiley‐Liss, Inc.
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