Histological and prognostic importance of CD44+/CD24+/EpCAM+ expression in clinical pancreatic cancer

被引:57
作者
Ohara, Yusuke [1 ]
Oda, Tatsuya [1 ]
Sugano, Masato [2 ]
Hashimoto, Shinji [1 ]
Enomoto, Tsuyoshi [1 ]
Yamada, Keiichi [1 ]
Akashi, Yoshimasa [1 ]
Miyamoto, Ryoichi [1 ]
Kobayashi, Akihiko [1 ]
Fukunaga, Kiyoshi [1 ]
Morishita, Yukio [2 ,3 ]
Ohkohchi, Nobuhiro [1 ]
机构
[1] Univ Tsukuba, Fac Med, Dept Surg, Div Gastroenterol & Hepatobiliary Surg & Organ Tr, Tsukuba, Ibaraki, Japan
[2] Univ Tsukuba, Fac Med, Dept Diagnost Pathol, Tsukuba, Ibaraki, Japan
[3] Tokyo Med Univ, Ibaraki Med Ctr, Dept Diagnost Pathol, Ami, Ibaraki, Japan
关键词
STEM-CELLS; SOLID TUMORS; IDENTIFICATION; CARCINOMA; CD133; ADENOCARCINOMAS; HETEROGENEITY; RESISTANCE; SURVIVAL; ANTIBODY;
D O I
10.1111/cas.12198
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD44(+)/CD24(+)/EpCAM(+) cells have been reported to be cancer stem cells in pancreatic cancer; however, the histological and clinical importance of these cells has not yet been investigated. Here we clarified the characteristics of CD44(+)/CD24(+)/EpCAM(+) cells in clinical specimens of pancreatic cancer using immunohistochemical assay. We used surgical specimens of pancreatic ductal adenocarcinoma from 101 patients. In view of tumor heterogeneity, we randomly selected 10 high-power fields per case, and triple-positive CD44(+)/CD24(+)/EpCAM(+) expression was identified using our scoring system. The distribution, histological characteristics, and prognostic importance of CD44(+)/CD24(+)/EpCAM(+) cells were then analyzed. As a result, the distribution of CD44(+)/CD24(+)/EpCAM(+) cells varied widely among the 101 cases examined, and CD44(+)/CD24(+)/EpCAM(+) expression was correlated with poor glandular differentiation and high proliferation. Survival analysis showed that CD44(+)/CD24(+)/EpCAM(+) expression was not correlated with patient outcome; however, CD44(+)/CD24(+) expression appeared to be correlated with poor prognosis. In conclusion, CD44(+)/CD24(+)/EpCAM(+) expression overlapped with poorly differentiated cells and possessed high proliferative potential in clinical pancreatic cancer. In particular, the presence of double-positive CD44(+)/CD24(+) expression seemed to have clinical relevance, associating with poor prognosis.
引用
收藏
页码:1127 / 1134
页数:8
相关论文
共 45 条
[1]   A proposal for a new and more practical grading scheme for pancreatic ductal adenocarcinoma [J].
Adsay, NV ;
Basturk, C ;
Bonnett, M ;
Kilinc, N ;
Andea, AA ;
Feng, JN ;
Che, MX ;
Aulicino, MR ;
Levi, E ;
Cheng, JD .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (06) :724-733
[2]   Ep-CAM is a significant prognostic factor in pancreatic cancer patients by suppressing cell activity [J].
Akita, H. ;
Nagano, H. ;
Takeda, Y. ;
Eguchi, H. ;
Wada, H. ;
Kobayashi, S. ;
Marubashi, S. ;
Tanemura, M. ;
Takahashi, H. ;
Ohigashi, H. ;
Tomita, Y. ;
Ishikawa, O. ;
Mori, M. ;
Doki, Y. .
ONCOGENE, 2011, 30 (31) :3468-3476
[3]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[4]  
[Anonymous], 2009, TNM classification of malignant tumours
[5]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[6]  
Buck AC, 2001, J NUCL MED, V42, P721
[7]   Stem cells, quiescence and rectal carcinoma: an unexplored relationship and potential therapeutic target [J].
Buczacki, S. ;
Davies, R. J. ;
Winton, D. J. .
BRITISH JOURNAL OF CANCER, 2011, 105 (09) :1253-1259
[8]   Recent advances in cancer stem cells [J].
Cho, Robert W. ;
Clarke, Michael F. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2008, 18 (01) :48-53
[9]  
Cui JH, 2001, WORLD J GASTROENTERO, V7, P381
[10]   Influence of pathological tumour variables on long-term survival in resectable gastric cancer [J].
Cuschieri, A ;
Talbot, IC ;
Weeden, S .
BRITISH JOURNAL OF CANCER, 2002, 86 (05) :674-679