Current Challenges and Opportunities for Chemoprevention of Pancreatic Cancer

被引:9
作者
Mohammed, Altaf [1 ,2 ]
Janakiram, Naveena B. [1 ]
Madka, Venkateshwar [1 ]
Li, Min [1 ]
Asch, Adam S. [1 ]
Rao, Chinthalapally V. [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Hem Onc Sect,Ctr Canc Prevent & Drug Dev, Oklahoma City, OK USA
[2] NCI, Dev Res Grp, Canc Prevent Div, Rockville, MD USA
关键词
Pancreatic cancer; chemoprevention; genetically engineered mouse models; early detection; targets; drug; invasive carcinoma; ENGINEERED MOUSE MODEL; INTRAEPITHELIAL NEOPLASIA; DUCTAL ADENOCARCINOMA; DELAY PROGRESSION; PREVENTS PROGRESSION; STEM-CELLS; RISK; CARCINOMA; INHIBITION; MUTATIONS;
D O I
10.2174/0929867324666170209104453
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The incidence of pancreatic cancer (PC) is rising in parallel with the deaths caused by this malignant disease largely due to limited improvement in current treatment strategies. In spite of aggressive PC research, for the past three decades, there has been no significant improvement in the five-year survival for this cancer. Like many other cancers, it takes several years for normal pancreatic cells to transform into pancreatic precursor lesions and to further progress into invasive carcinoma. Hence there is a scope for the development of chemo-preventive strategies to inhibit/delay/prevent progression of this disease into an advanced stage cancer. Objective: Chemoprevention of pancreatic cancer. Method: Review of published literature. Results and Conclusion: Availability of various genetically engineered mouse (GEM) models of PC has led to accelerated progress in understanding the disease and developing intervention strategies otherwise stalled for a long time. These GEM models spontaneously develop PC in a stepwise manner and mimic the disease etiology in humans. Understanding PC development from initiation to progression to metastasis is very important for early detection and prevention of PC. In this review, we focus on the current situation, the potential challenges, the progress in existing strategies and available opportunities as well as suggest key areas for research within the increasingly important area of pancreatic cancer chemoprevention.
引用
收藏
页码:2535 / 2544
页数:10
相关论文
共 70 条
[1]   Circulating miR-483-3p and miR-21 is highly expressed in plasma of pancreatic cancer [J].
Abue, Makoto ;
Yokoyama, Misa ;
Shibuya, Rie ;
Tamai, Keiichi ;
Yamaguchi, Kazunori ;
Sato, Ikuro ;
Tanaka, Nobuyuki ;
Hamada, Shin ;
Shimosegawa, Tooru ;
Sugamura, Kazuo ;
Satoh, Kennichi .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2015, 46 (02) :539-547
[2]   Activated Kras and Ink4a/Arf deficiency cooperate to produce metastatic pancreatic ductal adenocarcinoma [J].
Aguirre, AJ ;
Bardeesy, N ;
Sinha, M ;
Lopez, L ;
Tuveson, DA ;
Horner, J ;
Redston, MS ;
DePinho, RA .
GENES & DEVELOPMENT, 2003, 17 (24) :3112-3126
[3]  
ANDRENSANDBERG A, 1989, ACTA CHIR SCAND, P75
[4]  
[Anonymous], 2015, INT J CANCER, DOI DOI 10.1002/IJC.29210
[5]  
[Anonymous], 2016, CANC FACTS FIG
[6]  
BAECKSTROM D, 1991, J BIOL CHEM, V266, P21537
[7]   Inhibition of chronic pancreatitis and pancreatic intraepithelial neoplasia (PanIN) by capsaicin in LSL-KrasG12D/Pdx1-Cre mice [J].
Bai, Han ;
Li, Haonan ;
Zhang, Wanying ;
Matkowskyj, Kristina A. ;
Liao, Jie ;
Srivastava, Sanjay K. ;
Yang, Guang-Yu .
CARCINOGENESIS, 2011, 32 (11) :1689-1696
[8]   Both p16Ink4a and the p19Arf-p53 pathway constrain progression of pancreatic adenocarcinoma in the mouse [J].
Bardeesy, N ;
Aguirre, AJ ;
Chu, GC ;
Cheng, KH ;
Lopez, LV ;
Hezel, AF ;
Feng, B ;
Brennan, C ;
Weissleder, R ;
Mahmood, U ;
Hanahan, D ;
Redston, MS ;
Chin, L ;
DePinho, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (15) :5947-5952
[9]   Refinement of screening for familial pancreatic cancer [J].
Bartsch, D. K. ;
Slater, E. P. ;
Carrato, A. ;
Ibrahim, I. S. ;
Guillen-Ponce, C. ;
Vasen, H. F. A. ;
Matthaei, E. ;
Earl, J. ;
Jendryschek, F. S. ;
Figiel, J. ;
Steinkamp, M. ;
Ramaswamy, A. ;
Vazquez-Sequeiros, E. ;
Munoz-Beltran, M. ;
Montans, J. ;
Mocci, E. ;
Bonsing, B. A. ;
Wasser, M. ;
Kloeppel, G. ;
Langer, P. ;
Fendrich, V. ;
Gress, T. M. .
GUT, 2016, 65 (08) :1314-1321
[10]   Multiple small "imaging" branch-duct type intraductal papillary mucinous neoplasms (IPMNs) in familial pancreatic cancer: indicator for concomitant high grade pancreatic intraepithelial neoplasia? [J].
Bartsch, D. K. ;
Dietzel, K. ;
Bargello, M. ;
Matthaei, E. ;
Kloeppel, G. ;
Esposito, I. ;
Heverhagen, J. T. ;
Gress, T. M. ;
Slater, E. P. ;
Langer, P. .
FAMILIAL CANCER, 2013, 12 (01) :89-96