Blotta Simona, Tassone Pierfrancesco, Prabhala Rao H, Tagliaferri Piersandro, Cervi David, Amin Samir, Jakubikova Jana, Tai Yu-Tzu, Podar Klaus, Mitsiades Constantine S, Zullo Alessandro, Franco Brunella, Anderson Kenneth C, Munshi Nikhil C
Jerome Lipper Multiple Myeloma Center and LeBow Institute for Myeloma Therapeutics, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Blood. 2009 Oct 8;114(15):3276-84. doi: 10.1182/blood-2009-04-219436. Epub 2009 Jul 8.
The transformation from monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) is thought to be associated with changes in immune processes. We have therefore used serologic analysis of recombinant cDNA expression library to screen the sera of MGUS patients to identify tumor-associated antigens. A total of 10 antigens were identified, with specific antibody responses in MGUS. Responses appeared to be directed against intracellular proteins involved in cellular functions, such as apoptosis (SON, IFT57/HIPPI), DNA and RNA binding (ZNF292, GPATCH4), signal transduction regulators (AKAP11), transcriptional corepressor (IRF2BP2), developmental proteins (OFD1), and proteins of the ubiquitin-proteasome pathway (PSMC1). Importantly, the gene responsible for the oral-facial-digital type I syndrome (OFD1) had response in 6 of 29 (20.6%) MGUS patients but 0 of 11 newly diagnosed MM patients. Interestingly, 3 of 11 (27.2%) MM patients after autologous stem cell transplantations showed responses to OFD1. We have confirmed T-cell responses against OFD1 in MGUS and observed down-regulation of GLI1/PTCH1 and p-beta-catenin after OFD1 knock-down with specific siRNA, suggesting its functional role in the regulation of Hh and Wnt pathways. These findings demonstrate OFD1 as an important immune target and highlight its possible role in signal transduction and tumorigenesis in MGUS and MM.
意义未明的单克隆丙种球蛋白病(MGUS)向多发性骨髓瘤(MM)的转变被认为与免疫过程的变化有关。因此,我们使用重组cDNA表达文库的血清学分析来筛选MGUS患者的血清,以鉴定肿瘤相关抗原。共鉴定出10种抗原,MGUS患者中有特异性抗体反应。这些反应似乎针对参与细胞功能的细胞内蛋白质,如细胞凋亡(SON、IFT57/HIPPI)、DNA和RNA结合(ZNF292、GPATCH4)、信号转导调节因子(AKAP11)、转录共抑制因子(IRF2BP2)、发育蛋白(OFD1)以及泛素-蛋白酶体途径的蛋白质(PSMC1)。重要的是,导致口面指I型综合征(OFD1)的基因在29例MGUS患者中有6例(20.6%)出现反应,但在11例新诊断的MM患者中无反应。有趣的是,11例自体干细胞移植后的MM患者中有3例(27.2%)对OFD1有反应。我们已证实MGUS中针对OFD1的T细胞反应,并观察到用特异性siRNA敲低OFD1后GLI1/PTCH1和p-β-连环蛋白的下调,提示其在Hh和Wnt途径调节中的功能作用。这些发现证明OFD1是一个重要的免疫靶点,并突出了其在MGUS和MM的信号转导及肿瘤发生中的可能作用。