Associations between leptin and adiponectin receptor upregulation, visceral obesity and tumour stage in oesophageal and junctional adenocarcinoma

被引:70
作者
Howard, J. M. [2 ]
Beddy, P. [3 ]
Ennis, D. [2 ]
Keogan, M. [3 ]
Pidgeon, G. P. [2 ]
Reynolds, J. V. [1 ,2 ]
机构
[1] St James Hosp, Dept Surg, Trinity Ctr Hlth Sci, Dublin 8, Ireland
[2] Univ Dublin Trinity Coll, Dept Surg, Dublin 2, Ireland
[3] Univ Dublin Trinity Coll, Dept Radiol, Dublin 2, Ireland
关键词
COLORECTAL-CANCER RISK; PLASMA ADIPONECTIN; CELL-PROLIFERATION; PHYSICAL-ACTIVITY; BREAST-CANCER; IN-VITRO; EXPRESSION; GROWTH; ANGIOGENESIS; OVERWEIGHT;
D O I
10.1002/bjs.7072
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Obesity is associated with oesophageal adenocarcinoma, but mechanisms linking fat and carcinogenesis remain poorly understood. Altered circulating adipocytokines may be important. This study aimed to identify pathways through which visceral fist impacts on tumour biology. Methods: Seventy-five patients with oesophageal adenocarcinoma underwent anthropometric and radiological assessment of obesity. Expression of leptin receptor (ObR) and adiponectin receptors 1 and 2 (AdipR1; AdipR2) was quantified by real-time reverse transcriptase-polymerase chain reaction. The human oesophageal adenocarcinoma cell line OE33 was used as the calibrator sample. Results: Ninety-one per cent of tumours expressed ObR, 95 per cent expressed AdipR1 and 100 per cent expressed AdipR2. Relative expression of ObR was upregulated in 67 per cent, and AdipR1 and AdipR2 were downregulated in 55 and 68 per cent respectively, relative to the calibrator sample. Upregulated ObR and AdipR2 expression was significantly associated with anthropometric and radiological measures of obesity. Upregulated ObR was associated with advanced tumour and node category (P = 0.036 and P = 0.025 respectively), and upreg-ulated AdipR2 with nodal involvement (P = 0.037). Conclusion: Obesity is associated with upregulated ObR and AdipR2 expression in oesophageal adenocarcinoma. The association of ObR and AdipR2 with tumour stage suggest that pathways involving adipocytokines affect tumour biology.
引用
收藏
页码:1020 / 1027
页数:8
相关论文
共 48 条
[1]   The metabolic syndrome - a new worldwide definition [J].
Alberti, KGMM ;
Zimmet, P ;
Shaw, J .
LANCET, 2005, 366 (9491) :1059-1062
[2]  
[Anonymous], 2002, AJCC CANC STAG MAN
[3]   Leptin stimulates the proliferation of human colon cancer cells in vitro but does not promote the growth of colon cancer xenografts in nude mice or intestinal tumorigenesis in ApcMin/+ mice [J].
Aparicio, T ;
Kotelevets, L ;
Tsocas, A ;
Laigneau, JP ;
Sobhani, I ;
Chastre, E ;
Lehy, T .
GUT, 2005, 54 (08) :1136-1145
[4]  
*APPL BIOS, 1997, US B APPL BIOS, V2
[5]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[6]   ABDOMINAL COMPOSITION QUANTIFIED BY COMPUTED-TOMOGRAPHY [J].
BAUMGARTNER, RN ;
HEYMSFIELD, SB ;
ROCHE, AF ;
BERNARDINO, M .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1988, 48 (04) :936-945
[7]   Divergent signaling capacities of the long and short isoforms of the leptin receptor [J].
Bjorbaek, C ;
Uotani, S ;
da Silva, B ;
Flier, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (51) :32686-32695
[8]   Overweight, obesity, and mortality from cancer in a prospectively studied cohort of US adults [J].
Calle, EE ;
Rodriguez, C ;
Walker-Thurmond, K ;
Thun, MJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (17) :1625-1638
[9]   Adiponectin Deficiency Limits Tumor Vascularization in the MMTV-PyV-mT Mouse Model of Mammary Cancer [J].
Denzel, Martin S. ;
Hebbard, Lionel W. ;
Shostak, Gregory ;
Shapiro, Lawrence ;
Cardiff, Robert D. ;
Ranscht, Barbara .
CLINICAL CANCER RESEARCH, 2009, 15 (10) :3256-3264
[10]  
Despres Jean-Pierre, 1993, Nutrition Research Reviews, V6, P137, DOI 10.1079/NRR19930010