The use of molecular technology in the differentiation of pancreatic cancer and chronic pancreatitis

被引:18
作者
Bramhall, SR [1 ]
机构
[1] Univ Birmingham, Queen Elizabeth Hosp, Dept Surg, Birmingham B15 2TH, W Midlands, England
关键词
pancreatic cancer; chronic pancreatitis; molecular biology; differentiation;
D O I
10.1385/IJGC:23:2:83
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Conclusion. It is concluded that currently there are limitations in the use of some of the proposed tests, whereas in the future, further progress in our understanding of the molecular biology of pancreatic disease and the development and application of existing techniques should have a greater impact on clinical practice. Background, Fifteen to 20% of patients with pancreatic cancer present with a resectable mass in the head of the pancreas, but there is a subgroup of patients for whom it is difficult to reach the correct diagnosis. Method, This article addresses how molecular technology can be used to aid in the diagnosis of this group of patients. The clinical and scientific literature is reviewed by accessing papers through the Medline database. Results. This article reviews the limitations of conventional imaging techniques and the limitations of fine needle aspiration cytology and cytological examination of pancreatic duct secretions. The molecular biology of both pancreatic cancer and chronic pancreatitis is then reviewed with emphasis on the common molecular defects seen in these diseases. The current use of molecular techniques in the examination of cytological and histological specimens, stool, blood, and pancreatic duct secretions and how this helps discriminate between benign and malignant lesions of the pancreas is addressed. Finally, the use of novel serum screening tests in groups at high risk of pancreatic cancer is discussed.
引用
收藏
页码:83 / 100
页数:18
相关论文
共 205 条
[11]   EXPRESSION OF AND RESPONSE TO GROWTH REGULATORY PEPTIDES BY 2 HUMAN PANCREATIC-CARCINOMA CELL-LINES [J].
BEAUCHAMP, RD ;
LYONS, RM ;
YANG, EY ;
COFFEY, RJ ;
MOSES, HL .
PANCREAS, 1990, 5 (04) :369-380
[12]  
BERGMANN U, 1995, CANCER RES, V55, P2007
[13]   INSULIN-LIKE GROWTH FACTOR-I (IGF-I)-BINDING PROTEIN COMPLEX IS A BETTER MITOGEN THAN FREE IGF-I [J].
BLUM, WF ;
JENNE, EW ;
REPPIN, F ;
KIETZMANN, K ;
RANKE, MB ;
BIERICH, JR .
ENDOCRINOLOGY, 1989, 125 (02) :766-772
[14]   CYTOLOGICAL DIAGNOSIS OF PANCREATIC TUMORS [J].
BODNER, E ;
SCHWAMBERGER, K ;
MIKUZ, G .
WORLD JOURNAL OF SURGERY, 1982, 6 (01) :103-106
[15]  
BOS JL, 1989, CANCER RES, V49, P4682
[16]   LOSS OF HETEROZYGOSITY INVOLVING THE APC AND MCC GENETIC-LOCI OCCURS IN THE MAJORITY OF HUMAN ESOPHAGEAL CANCERS [J].
BOYNTON, RF ;
BLOUNT, PL ;
YIN, J ;
BROWN, VL ;
HUANG, Y ;
TONG, Y ;
MCDANIEL, T ;
NEWKIRK, C ;
RESAU, JH ;
RASKIND, WH ;
HAGGITT, RC ;
REID, BJ ;
MELTZER, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3385-3388
[17]   TREATMENT AND SURVIVAL IN 13560 PATIENTS WITH PANCREATIC-CANCER, AND INCIDENCE OF THE DISEASE, IN THE WEST MIDLANDS - AN EPIDEMIOLOGIC-STUDY [J].
BRAMHALL, SR ;
ALLUM, WH ;
JONES, AG ;
ALLWOOD, A ;
CUMMINS, C ;
NEOPTOLEMOS, JP .
BRITISH JOURNAL OF SURGERY, 1995, 82 (01) :111-115
[18]   TRANSFORMING GROWTH FACTOR-BETA-1 IS PRESENT AT SITES OF EXTRACELLULAR-MATRIX GENE-EXPRESSION IN HUMAN PULMONARY FIBROSIS [J].
BROEKELMANN, TJ ;
LIMPER, AH ;
COLBY, TV ;
MCDONALD, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6642-6646
[19]  
BURMER GC, 1989, CANCER RES, V49, P2141
[20]   FREQUENT SOMATIC MUTATIONS AND HOMOZYGOUS DELETIONS OF THE P16 (MTS1) GENE IN PANCREATIC ADENOCARCINOMA [J].
CALDAS, C ;
HAHN, SA ;
DACOSTA, LT ;
REDSTON, MS ;
SCHUTTE, M ;
SEYMOUR, AB ;
WEINSTEIN, CL ;
HRUBAN, RH ;
YEO, CJ ;
KERN, SE .
NATURE GENETICS, 1994, 8 (01) :27-32