Modulation of c-kit expression in pancreatic adenocarcinoma: A novel stem cell marker responsible for the progression of the disease

被引:10
作者
Amsterdam, Abraham [1 ]
Raanan, Calanit [2 ]
Polin, Nava [1 ]
Melzer, Ehud [3 ]
Givol, David [1 ]
Schreiber, Letizia [4 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Biol Serv, IL-76100 Rehovot, Israel
[3] Kaplan Med Ctr, Dept Gastroenterol, IL-76100 Rehovot, Israel
[4] Wolfson Govt Hosp, IL-58100 Holon, Israel
关键词
Insulin; Diabetes; beta cells; KRAS; LGR5; Nanog; GASTROINTESTINAL STROMAL TUMORS; TYROSINE KINASE; OVARIAN-CANCER; BETA-CELLS; MUTATIONS; DIFFERENTIATION; LOCALIZATION; SORAFENIB; PROGNOSIS; CARCINOMA;
D O I
10.1016/j.acthis.2013.07.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal cancers because of late symptoms and resistance to chemotherapy and radiation therapy. We have investigated the appearance of c-kit, a stem cell marker, in both normal adult pancreatic tissue and in cancerous tissue. Apart from some very pale staining of islets of Langerhans, normal pancreas was devoid of staining with antibodies to c-kit. In contrast, in cancerous tissue that still preserves the overall integrity of the pancreatic tissue, there was a clear labeling in islets of Langerhans, which seemed to be co-localized with insulin containing beta cells. In other cases, where the pancreatic tissue was completely deteriorated, intensive labeling was clearly evident in remnants of both the exocrine and the endocrine tissues. The duct cells of the adenocarcinoma were moderately but clearly labeled with antibodies to c-kit. In contrast, in metastasis of PDAC, very intensive labeling of c-kit was evident. The location of KRAS, which is strongly associated with PDAC, was also analyzed at the initial stages of the disease, when islets of Langerhans still preserve their integrity to a large extent. KRAS was found exclusively in islets of Langerhans and overlapped in its location with insulin and c-kit expressing cells. It is suggested that the modulation of the expression of c-kit, visualized by antibodies to the oncogene molecule, may play an important role in the formation and progression of PDAC. The absence of c-kit in normal pancreas and its appearance in PDAC is probably due to a mutational event, which probably allows conversion of the beta cells into cancer stem cells (CSC). Co-expression of both c-kit and KRAS, typical markers for CSC with overlapping with insulin in islets of Langerhans, strongly support the notion that beta-cells play a central role in the development of PDAC. The use of specific drugs that can attenuate the kinase activity of c-kit or target KRAS expressing cancer cells should be tested in order to attenuate the progression of this lethal disease. (C) 2013 Published by Elsevier GmbH.
引用
收藏
页码:197 / 203
页数:7
相关论文
共 36 条
[1]   Differential localization of LGR5 and Nanog in clusters of colon cancer stem cells [J].
Amsterdam, Abraham ;
Raanan, Calanit ;
Schreiber, Letizia ;
Freyhan, Ora ;
Fabrikant, Yakov ;
Melzer, Ehud ;
Givol, David .
ACTA HISTOCHEMICA, 2013, 115 (04) :320-329
[2]   LGR5 and Nanog identify stem cell signature of pancreas beta cells which initiate pancreatic cancer [J].
Amsterdam, Abraham ;
Raanan, Calanit ;
Schreiber, Letizia ;
Polin, Nava ;
Givol, David .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 433 (02) :157-162
[3]  
[Anonymous], 2012, EXP CELL RES, V318
[4]   Targeted therapy of cancer: new roles for pathologists in identifying GISTs and other sarcomas [J].
Antonescu, Cristina R. .
MODERN PATHOLOGY, 2008, 21 :S31-S36
[5]   Therapeutic targeting of c-KIT in cancer [J].
Ashman, Leonie K. ;
Griffith, Renate .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2013, 22 (01) :103-115
[6]   Determination of drug synergism between the tyrosine kinase inhibitors NSC 680410 (adaphostin) and/or STI571 (imatinib mesylate, Gleevec) with cytotoxic drugs against human leukemia cell lines [J].
Avramis, IA ;
Laug, WE ;
Sausville, EA ;
Avramis, VI .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2003, 52 (04) :307-318
[7]   Stem cells as the root of pancreatic ductal adenocarcinoma [J].
Balic, Anamaria ;
Dorado, Jorge ;
Alonso-Gomez, Mercedes ;
Heeschen, Christopher .
EXPERIMENTAL CELL RESEARCH, 2012, 318 (06) :691-704
[8]   CD117/KIT expression in pancreatic adenocarcinoma [J].
Bateman, Adrian C. ;
Judd, Mary ;
Radenkovic, Dejan ;
Johnson, Colin D. .
PANCREAS, 2008, 36 (01) :76-79
[9]   Ovarian cancer stem cell markers: Prognostic and therapeutic implications [J].
Burgos-Ojeda, Daniela ;
Rueda, Bo R. ;
Buckanovich, Ronald J. .
CANCER LETTERS, 2012, 322 (01) :1-7
[10]   Evidence for cancer stem cells contributing to the pathogenesis of ovarian cancer [J].
Curley, Michael D. ;
Garrett, Leslie A. ;
Schorge, John O. ;
Foster, Rosemary ;
Rueda, Bo R. .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2011, 16 :368-392