{A figure is presented}Does Early Colectomy Increase Desmoid Risk in Familial Adenomatous Polyposis?

Clinical Gastroenterology and Hepatology

Volumn 5, Issue 10, 2007, Pages 1190-1194

  Durno, Carol ^a,b   Monga, Neerav ^a   Bapat, Bharati ^a   Berk, Theresa ^a   Cohen, Zane ^a   Gallinger, Steven ^a  

^a MOUNT SINAI HOSPITAL   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOMATOUS POLYP; ADOLESCENT; ADULT; AGED; APC GENE; ARTICLE; CANADA; CAUSE OF DEATH; CODON; COLON RESECTION; DESMOID TUMOR; DISEASE ASSOCIATION; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; GENDER; GENE; GENE MUTATION; HIGH RISK POPULATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MORTALITY; RISK FACTOR; ABDOMINAL TUMOR; AGE; CLINICAL TRIAL; COLON POLYPOSIS; CONFIDENCE INTERVAL; FIBROMATOSIS; FOLLOW UP; GASTROINTESTINAL ENDOSCOPY; GENETICS; MIDDLE AGED; MULTICENTER STUDY; MUTATION; PHYSIOLOGY; PREVALENCE; PROGNOSIS; RETROSPECTIVE STUDY; SEX DIFFERENCE; SURVIVAL RATE; TIME; TUMOR SUPPRESSOR GENE;

ABDOMINAL NEOPLASMS; ADENOMATOUS POLYPOSIS COLI; ADOLESCENT; ADULT; AGE FACTORS; AGED; COLECTOMY; CONFIDENCE INTERVALS; ENDOSCOPY, GASTROINTESTINAL; FEMALE; FIBROMATOSIS, AGGRESSIVE; FOLLOW-UP STUDIES; GENES, APC; HUMANS; MALE; MIDDLE AGED; MUTATION; ONTARIO; PREVALENCE; PROGNOSIS; RETROSPECTIVE STUDIES; RISK FACTORS; SEX FACTORS; SURVIVAL RATE; TIME FACTORS;

EID: 34748883309     PISSN: 15423565     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cgh.2007.06.010     Document Type: Article

References (50)

1. Fletcher C.D.M., and Mertens F. World Health Organization classification of tumors: pathology and genetics of tumors of soft tissue and bone. In: Fletch C.D.M., Uni K.K., and Mertens F. (Eds) (2002), IARC Press, Lyon, France 48-49 83-84
2. Gurbuz A.K., Giardiello F.M., Petersen G.M., et al. Desmoid tumours in familial adenomatous polyposis. Gut 35 (1994) 377-381
3. Sturt N.J.H., and Clark S.K. Current ideas in desmoid tumours. Familial Cancer 5 (2006) 275-285
4. Caspari R., Olschwang S., Friedl W., et al. Familial adenomatous polyposis:desmoids tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444. Human Mol Genet 4 (1995) 337-340
5. Davies D.R., Armstrong J.G., Thakker N., et al. Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene. Am J Hum Genet 57 (1995) 1151-1158
6. Scott R.J., Froggatt N.J., Trembath R.C., et al. Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3′ APC gene mutation. Hum Mol Genet 5 (1996) 1921-1924
7. Miyaki M., Konishi M., Kikuchi-Yanoshita R., et al. Coexistence of somatic and germ-line mutations of APC gene in desmoid tumours from patients with familial adenomatous polyposis. Cancer Res 53 (1993) 5070-5082
8. Palmirotta R., Curia M.C., Esposito D.L., et al. Novel mutations and inactivation of both alleles of the APC gene in desmoid tumours. Hum Mol Genet 4 (1995) 1979-1981
9. Sturt N.J.H., Gallagher M.C., Bassett P., et al. Evidence for genetic predisposition to desmoid tumours in familial adenomatous polyposis independent of the germline APC mutation. Gut 53 (2004) 1832-1836
10. Friedl W., Caspari R., Sengteller M., et al. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis?. experience from 680 FAP families. Gut 46 (2001) 515-521
11. Clark S.K., Neale K.F., Landgrebe J.C., et al. Desmoid tumours complicating familial adenomatous polyposis. Br J Surg 86 (1999) 1185-1189
12. Bertario L., Russo A., Sala P., et al. Genotype and phenotype factors as determinants of desmoid tumours in patients with familial adenomatous polyposis. Int J Cancer 95 (2001) 102-107
13. Soravia C., Berk T., McLeod R.S., et al. Desmoid disease in patients with familial adenomatous polyposis. Dis Colon Rectum 43 (2000) 363-369
14. Clark S.K., and Phillips R.K.S. Desmoids in familial adenomatous polyposis. Br J Surg 83 (1996) 1494-1504
15. Hartley J.E., Church J.M., Gupta S., et al. Significance of incidential desmoids identified during surgery for familial adenomatous polyposis. Dis Colon Rectum 47 (2004) 334-338
16. Heiskanen I., and Jarvinen H.J. Occurrence of desmoid tumours in familial adenomatous polyposis and results of treatment. Int J Colorect Dis 11 (1996) 157-162
17. Winawer S., Fletcher R., Rex D., et al. Colorectal cancer screening and surveillance: clinical guidelines and rationale-update based on new evidence. Gastroenterology 124 (2003) 544-560
18. Couture J., Mitri A., Lagace R., et al. A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor. Clin Genet 57 (2000) 205-212
19. Kaplan E.L., and Meier P. Nonparametric estimation from incomplete observations. J Am Stat Assoc 53 (1958) 457-481
20. Cox D.R. Regression models and life tables. J Roy Statist Soc 34 (1972) 187
21. Hansmann A., Adolph C., Vogel T., et al. High-dose tamoxifen and sulindac as first-line treatment for desmoid tumors. Cancer 100 (2004) 612-620
22. Poritz L.S., Blackstein M., Berk T., et al. Extended follow-up of patients treated with cytotoxic chemotherapy for intra-abdominal desmoid tumors. Dis Colon Rectum 44 (2001) 1268-1273
23. Church J., Berk T., Boman B.M., et al. Staging intra-abdominal desmoid tumors in familial adenomatous polyposis: a search for a uniform approach to a troubling disease. Dis Colon Rectum 48 (2005) 1528-1534
24. Eagel B.A., Zentler-Munro P., and Smith I.E. Mesenteric desmoid tumours in Gardner's syndrome: review of medical treatments. Postgrad Med J 65 (1989) 497-501
25. Lofti A.K., Dozois R.R., Gordon H., et al. Mesenteric fibromatosis complicatinf familial adenomatous polyposis: predisposing factors and results of treatment. Int J Colorectal Dis 4 (1989) 30-36
26. Bertario L., Russo A., Sala P., et al. Genotype and phenotype factor as determinants of desmoid tumors in patients with familial adenomatous polyposis. Int J Cancer 95 (2001) 102-107
27. Church J.M. Anatomy of a gene: functional correlations of APC mutation. Semin Colon Rectal Surg 9 (1998) 49-52
28. Nagase H., Miyoshi Y., Horri A., et al. Correlation between the location of germline mutations in the APC gene and the number of colorectal polyps in familial adenomatous polyposis coli. Cancer Res 52 (1992) 4055-4057
29. van der Luijt R.B., Meera Khan P., Vasen H.F.A., et al. Germline mutations in the 3′ part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli. Hum Genet 98 (1996) 727-734
30. Soravia C., Berk T., Madlensky L., et al. Genotype-phenotype correlations in attenuated adenomatous polyposis. Am J Hum Genet 62 (1998) 1290-1301
31. Couture J., Mitri A., Lagace R., et al. A germline mutation at the extreme 3′ end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor. Clin Gen 57 (2000) 205-212
32. Gardner R.J., Kool D., Edkins E., et al. The clinical correlates of a 3′ truncating mutation (codons 1982-1983) in the adenomatous polyposis coli gene. Gastroenterology 113 (1997) 326-331
33. Eccles D., van der Luijt R., Breukel C., et al. Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. Am J Hum Genet 59 (1996) 1193-1201
34. Esplen M.J., Berk T., Butler K., et al. Quality of life in adults diagnosed with familial adenomatous polyposis and desmoid tumor. Dis Colon Rectum 47 (2004) 687-696
35. Ferrans C.E., and Powers M.J. Psychometric assessment of the quality of life index. Res Nursing Health 15 (1992) 29-38
36. Clark S.K., Johnson Smith T.G.P., Katz D.E., et al. Identification and progression of a desmoid precursor lesion in patients with familial adenomatous polyposis. Br J Surg 85 (1998) 970-973
37. Tonelli F., Valanzano R., and Brandi M.L. Pharmacologic treatment of desmoid tumors in familial adenomatous polyposis: results of an in vitro study 115 (1994) 473-479
38. Maseelall P., Robins J.C., Williams D.B., et al. Stabilization and regression of a recurrent desmoid tumor with the antiestrogen toremifene. Fertil Steril 84 (2005) 509
39. Leithner A., Gapp M., Radl R., et al. Immunohistochemical analysis of desmoid tumours. J Clin Pathol 58 (2005) 1152-1156
40. Heinrich M.C., McArthur G.A., Demetri G.D., et al. Clinical and molecular studies of the effect of imatinib on advanced aggressive fibromatosis (desmoid tumor). J Clin Oncol 24 (2006) 1195-1203
41. Church J., and McGannon E. Prior pregnancy ameliorates the course of intra-abdominal desmoid tumors in patients with familial adenomatous polyposis. Dis Colon Rectum 43 (2000) 445-450
42. Munemitsu S., Albert I., Souza B., et al. Regulation of intracellular beta-catenin levels by the adenomatous polyposis coli (APC) tumor-suppressor protein. Proc Natl Acad Sci U S A 92 (1995) 3046-3050
43. Behrens J., von Kries J.P., Kuhl M., et al. Functional interaction of beta-catenin with the transcription factor LEF-1. Nature 382 (1996) 638-642
44. Morin P.J., Sparks A.B., Korinek V., et al. Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC. Science 275 (1997) 1787-1790
45. Denys H., De Wever O., Nusgens B., et al. Invasion and MMP expression profile in desmoid tumours. Br J Cancer 90 (2004) 1443-1449
46. Amini Nik S., Hohenstein P., Jadidizaheh A., et al. Upregulation of Wilms' tumor gene 1 (WT1) in desmoid tumors. Int J Cancer 114 (2004) 202-208
47. Tolg C., Poon R., Fodde R., et al. Genetic deletion of receptor for hyaluronan-mediated motility (Rhamm) attenuates the formation of aggressive fibromatosis (desmoid tumor). Oncogene 22 (2003) 6873-6882
48. Bacac M., Migliavacca E., Stehle J.-C., et al. A gene expression signature that distinguishes desmoid tumours from nodular fasciitis. J Pathol 208 (2006) 543-553
49. Latchford A., Volikos E., Johnson V., et al. APC mutations in FAP-associated desmoid tumours are non-random but not 'just right'. Hum Mol Genet 16 (2007) 78-82
50. Martinico S.C.M., Jezzard S., Sturt N.J.H., et al. Assessment of endostation gene therapy for familial adenomatous polyposis-related desmoid tumors. Cancer Res 66 (2006) 8233-8240