García-Pravia Carmen, Galván José A, Gutiérrez-Corral Natalia, Solar-García Lorena, García-Pérez Eva, García-Ocaña Marcos, Del Amo-Iribarren Jokin, Menéndez-Rodríguez Primitiva, García-García Juan, de Los Toyos Juan R, Simón-Buela Laureano, Barneo Luis
Pathological Anatomy Service, Hospital Universitario Central de Asturias (HUCA), Oviedo, Spain ; Instituto Universitario de Oncología del Principado de Asturias (IUOPA), Oviedo, Spain.
PLoS One. 2013 Oct 23;8(10):e78327. doi: 10.1371/journal.pone.0078327. eCollection 2013.
The collagen11A1 (COL11A1) gene is overexpressed in pancreatic cancer. The expression of COL11A1 protein could be involved in desmoplastic events in pancreatic cancer, but an antibody that specifically stains the COL11A1 protein is not currently available.
A total of 54 pancreatic ductal adenocarcinomas (PDAC), 23 chronic pancreatitis (CP) samples, and cultured peritumoral stromal cells of PDAC (passages 3-6) were studied. Normal human pancreas tissue samples were obtained through a cadaveric organ donation program. 1) Validation of COL11A1 gene overexpression by q-RT-PCR.
the expression of COL11A1 gene is significantly increased in PDAC samples vs. normal and CP samples. 2) Analysis of COL11A1 by immunohistochemistry using highly specific anti-proCOL11A1 antibodies.
anti-proCOL11A1 stains stromal cells/cancer-associated fibroblasts (CAFs) of PDAC but it does not stain chronic benign condition (chronic pancreatitis) stromal cells, epithelial cells, or normal fibroblasts. 3) Evaluation of the discrimination ability of the antibody.
anti-proCOL11A1 immunostaining accurately discriminates between PDAC and CP (AUC 0.936, 95% CI 0.851, 0.981). 4) Phenotypic characterization of proCOL11A1+ stromal cells co-staining with mesenchymal, epithelial and stellate cell markers on pancreatic tissue samples and cultured peritumoral pancreatic cancer stromal cells.
ProCOL11A1+ cells present co-staining with mesenchymal, stellate and epithelial markers (EMT phenotype) in different proportions.
CONCLUSIONS/SIGNIFICANCE: Detection of proCOL11A1 through immunostaining with this newly-developed antibody allows for a highly accurate distinction between PDAC and CP. Unlike other available antibodies commonly used to detect CAFs, anti-proCOL11A1 is negative in stromal cells of the normal pancreas and almost absent in benign inflammation. These results strongly suggest that proCOL11A1 is a specific marker for CAFs, and thus, anti-proCOL11A1 is a powerful new tool for cancer research and clinical diagnostics.
胶原蛋白11A1(COL11A1)基因在胰腺癌中过表达。COL11A1蛋白的表达可能参与胰腺癌的促纤维增生过程,但目前尚无特异性标记COL11A1蛋白的抗体。
共研究了54例胰腺导管腺癌(PDAC)、23例慢性胰腺炎(CP)样本以及培养的PDAC瘤周基质细胞(第3 - 6代)。通过尸体器官捐赠项目获取正常人胰腺组织样本。1)采用q - RT - PCR验证COL11A1基因过表达。
与正常和CP样本相比,PDAC样本中COL11A1基因的表达显著增加。2)使用高度特异性的抗前胶原蛋白11A1(anti - proCOL11A1)抗体通过免疫组织化学分析COL11A1。
anti - proCOL11A1可标记PDAC的基质细胞/癌症相关成纤维细胞(CAF),但不标记慢性良性疾病(慢性胰腺炎)的基质细胞、上皮细胞或正常成纤维细胞。3)评估该抗体的鉴别能力。
anti - proCOL11A1免疫染色可准确区分PDAC和CP(曲线下面积0.936,95%置信区间0.851,0.981)。4)对胰腺组织样本和培养的PDAC瘤周基质细胞中与间充质、上皮和星状细胞标志物共染色的前胶原蛋白11A1阳性(proCOL11A1 +)基质细胞进行表型特征分析。
ProCOL11A1 +细胞呈现不同比例的与间充质、星状和上皮标志物的共染色(上皮 - 间质转化表型)。
结论/意义:使用这种新开发的抗体通过免疫染色检测前胶原蛋白11A1可实现PDAC和CP之间的高度准确区分。与其他常用于检测CAF的现有抗体不同,anti - proCOL11A1在正常胰腺的基质细胞中呈阴性,在良性炎症中几乎不存在。这些结果强烈表明前胶原蛋白11A1是CAF的特异性标志物,因此,anti - proCOL11A1是癌症研究和临床诊断的有力新工具。