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BRAF and KRAS Mutations in Colorectal Hyperplastic Polyps and Serrated Adenomas¹

Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Hong Kong [T. L. C., W. Z., S. Y. L., S. T. Y.], and Cancer Genome Project, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, CB10 1SA, United Kingdom

	ABSTRACT

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Colorectal cancer is believed to progress through an adenoma–carcinoma sequence. However, recent evidence increasingly supports the existence of an alternative route for colorectal carcinogenesis through serrated polyps, a group that encompasses a morphological spectrum, including hyperplastic polyp (HP), admixed hyperplastic polyp/adenoma (HP/AD), and serrated adenoma (SA; the latter two manifest epithelial dysplasia). We have studied a large series of serrated polyps for BRAF and KRAS mutations. BRAF mutations were detected in 18 of 50 (36%) HPs, 2 of 10 (20%) HP/ADs, and 9 of 9 (100%) SAs. Twenty-six of 29 mutations caused amino acid substitutions at valine 599, the known hotspot. KRAS mutations were detected in 9 of 50 (18%) HPs, 6 of 10 (60%) HP/ADs, and 0 of 9 (0%) SAs. BRAF and KRAS mutations are mutually exclusive (P = 0.001). The associations of BRAF mutations with SAs (P < 0.001) and KRAS mutations with HP/ADs (P = 0.005) are statistically significant. A majority (90%) of the serrated polyps showing dysplasia had mutations in either BRAF or KRAS, significantly different from those without dysplasia (54%; P = 0.014). Our data highlight the important role of activation of the RAS-RAF-mitogen-activated protein/extracellular signal-regulated kinase kinase-extracellular signal-regulated kinase-mitogen-activated protein kinase pathway in the initiation and progression of serrated neoplasms. Acquisition of a BRAF mutation appears to be associated with the progression of HP to SA, whereas progression to HP/AD is predominantly associated with acquisition of a KRAS mutation. The high incidence of BRAF mutations in HPs and SAs is consistent with the notion that the group of colorectal cancers carrying BRAF mutations may harbor most that have progressed through the HP-SA-carcinoma pathway.

	INTRODUCTION

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RAS proteins participate in the RAS-RAF-MEK³ -ERK-MAP kinase pathway, which mediates cellular responses to growth signals (1) . Somatic mutations of the RAS genes, leading to activation of this signaling pathway and malignant transformation, are common in human cancers. There are three RAF genes, each encoding cytoplasmic serine/threonine kinases that are regulated by binding to RAS (1 , 2) . We have shown previously that mutations of BRAF provide an alternative route for activation of this signaling pathway in human cancers (3) . BRAF mutations can be found in malignant melanoma, colorectal cancers, and ovarian borderline (low malignant potential) tumors, and they tend to occur in a mutually exclusive relationship with RAS mutations (3, 4, 5) . Subsequently, BRAF mutations have also been found in most benign melanocytic naevi and lung cancer (6, 7, 8) . Mutations in BRAF occur in two regions of the BRAF kinase domain, the activation segment (which protects the substrate binding site), and, less commonly, the G loop (which mediates binding of ATP). Mutated forms of BRAF that have been studied thus far have elevated kinase activity and can transform NIH3T3 cells (3) .

An adenoma–carcinoma sequence has long been recognized to constitute a major pathway of colorectal carcinogenesis (9) . KRAS is known to play an important role in the progression along this pathway, predominantly occurring during the transformation of small to intermediate sized adenomas (10) . We and others have demonstrated the involvement of BRAF in a similar phase of colorectal cancer development, albeit in a much smaller percentage of cases (3–10% of adenomas have BRAF mutations compared with 30–60% with KRAS mutations; Refs. 4 and 5 ). Emerging evidence supports the existence of an alternative pathway of colorectal cancer development through the serrated polyp (for review, see Refs. 11 and 12 ). The serrated polyp encompasses a morphological spectrum, including HPs, HP/ADs, and SAs. HPs of the large intestine are found in 12% of individuals >50 years of age (13 , 14) . Morphologically, they are characterized by elongated crypts with serrated architecture covered by nondysplastic colonic epithelial cells. It has been suggested that HPs arise because of hypermaturation of glandular cells consequent on diminished apoptosis (15) , but their pathogenesis and propensity for malignant progression remain controversial. Subsequently, two morphological variants of HPs that are associated with epithelial dysplasia have been recognized. The term SA has been used for polyps with serrated morphology (as seen in ordinary HPs) that show epithelial dysplasia throughout the lesion. HP/ADs show focal hyperplastic and focal adenomatous components (16 , 17) . Evolution of these lesions to invasive carcinomas has been reported (18, 19, 20, 21) .

Molecular studies have indicated that serrated polyps (including HPs) are likely to be clonal neoplasms, because mutations of KRAS and p53, MSI, and chromosome 1p loss have been found in variable proportions (22, 23, 24, 25, 26, 27, 28, 29, 30) . However, mutations of adenomatous polyposis coli are uncommon (26 , 30 , 31) . Overall, the molecular pathway of evolution in serrated polyps and its relative contribution to the incidence of colorectal cancer are unclear.

In our recent study of BRAF and KRAS mutations in colorectal polyps, one of three HPs showed a BRAF mutation (4) . This finding has prompted us to examine a larger series of serrated polyps for BRAF and KRAS mutations with reference to their morphological classification, in particular the presence of dysplasia and MSI.

	MATERIALS AND METHODS

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Materials.
Pathology records and histological slides with a diagnosis of either HP, HP/AD, or SA from 1997 to 2002 in the Department of Pathology, Queen Mary Hospital were reviewed independently by two pathologists with an interest in gastrointestinal neoplasia (S. Y. L. and S. T. Y.). Six-µm-thick sections were cut from paraffin-embedded tissue and stained with 0.1% methylene blue. The lesions were microdissected under a light microscope, and only areas with the pathological lesion were taken for DNA extraction. Apart from scanty amounts of contaminating inflammatory and stromal cells, we estimated that 70% of the resulting DNA was from the epithelial components of the serrated polyps. DNA was extracted using standard protocols. In total, 69 sporadic serrated polyps from 63 individuals generated adequate DNA of quality suitable for BRAF and KRAS analysis. This study was approved by the Ethics Committee of the University of Hong Kong.

Mutation Screening of BRAF and KRAS.
The complete coding sequences of exons 11 (G loop region) and 15 (activation segment) of BRAF and exon 2 of KRAS were amplified using intronic primers and directly sequenced on both strands using the DYEnamic ET Terminator Cycle Sequencing Kits (Amersham Pharmacia) and analyzed by the Applied Biosystems 377 or 3700 automated sequencer. These covered most of the mutation hot spots known previously of the two genes. All mutations were reconfirmed by independent PCR reactions and sequencing. The primers for BRAF sequencing of exon 15 were similar as described previously (3) . The primers for exon 11 of BRAF (forward- TTC TGT TTG GCT TGA CTT GAC TT and reverse- ACT TGT CAC AAT GTC ACC ACA TT) and exon 2 of KRAS (forward- CTG AAA ATG ACT GAA TAT AAA CTT GT and reverse- ATA TGC ATA TTA AAA CAA GAT TTA CC) were designed to amplify a shorter fragment suitable for use in paraffin DNA. In each case with mutation, the percentage of mutant population was estimated by the quotient of mutant peak height over mutant plus wild-type peak height.

Analysis of MSI.
Because corresponding normal tissue was not available, microsatellite analysis was performed using three monomorphic microsatellite markers, including BAT25, BAT26, and transforming growth factor ßR II. The procedure was similar to those described in our previous publications (4 , 32) .

Statistical Analysis.
Categorical variables were compared with the use of the ² test with Yates correction or Fisher’s exact test as appropriate.

	RESULTS

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Sixty-nine sporadic serrated polyps from 63 patients were suitable for the present study. These included 50 typical HPs, 10 HP/ADs, and 9 SAs. Thirty-nine polyps were from male patients, and 30 were from female patients. Twenty-two were from the right colon, and 46 were from the left colon (the tumor location in one case was not known). The 50 HPs showed no epithelial cell dysplasia. Of the 19 HP/ADs and SAs, 14 showed mild, 4 moderate, and 1 severe dysplasia. The size of these polyps ranged from 2 to 20 mm in maximal dimension (mean = 6.57 mm).

The incidence of BRAF and KRAS mutations and their relationship to clinicopathological features is shown in Table 1 . Of the 69 serrated polyps studied, there were 29 cases (42%) with BRAF mutations and 15 cases (21.7%) with KRAS mutations. The spectra of BRAF and KRAS mutations found are shown in Table 2 . Representative sequence chromatographs are shown in Fig. 1 . Twenty-eight of the 29 BRAF mutations are in exon 15 with only one located within exon 11, and 26 involve codon 599 (25 V599E, 1 V599M), shown previously to be a mutation hot spot. The other BRAF mutations are G468A, D586E, and F594L. The V599M and D586E are novel mutations that have not been reported before. In 72% of cases with BRAF mutation, the mutant allele constitutes 35–66% of the total mutant and wild-type signal, suggesting that these are heterozygous mutations present in most of the epithelial cells within the lesion. The remaining eight cases harbor mutant BRAF alleles that account for 20–32% of the total signal. The five cases with the lowest percentage of mutant alleles (20–24%) are all HPs. It is likely that these lower signals represent mutations present in a subpopulation of the lesion. For the 15 serrated polyps with KRAS mutations, the percentage of mutant alleles ranged from 20 to 71%. None of the polyps that carry a BRAF mutation have a KRAS mutation (P = 0.001, ² with Yates correction).

View larger version (29K): [in this window] [in a new window] [Download PPT slide]   Fig. 1. Sequence chromatographs of serrated polyps with BRAF or KRAS mutations. A, a SA with V599E (T1796A) mutation of BRAF. B, an HP without BRAF mutation. C, an SA with V599M (G1795A) mutation of BRAF. D, an HP with D586E (C1758G) mutation of BRAF. F, an admixed HP/AD with G12D (G35A) mutation of KRAS. G, an HP with no KRAS mutation.

	DISCUSSION

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We have shown that BRAF mutations are present in 42% of serrated polyps. Similar to most other tumors, conversion of valine 599 to glutamic acid is the most common mutation found in serrated polyps (86% of mutations observed). This substitution results in the insertion of a negatively charged residue adjacent to a site of regulatory phosphorylation at T598 which may mimic normal regulatory phosphorylation and lead to constitutive activation of BRAF independent of RAS. KRAS and BRAF mutations appear to be mutually exclusive, confirming previous suggestions that they have similar biological consequences (3, 4, 5) . The combined incidence of BRAF and KRAS mutations in serrated polyps is 64%, indicating that activation of the RAS-RAF-MEK-ERK-MAP kinase pathway constitutes a highly significant event in the pathogenesis of this group of lesions. The occurrence of either BRAF or KRAS mutations in 54% of otherwise histologically "innocuous" HPs suggests that these may be early steps in the initiation of the serrated neoplasia pathway. However, the presence of epithelial dysplasia is associated with even higher rates (90%) of mutation in either BRAF or KRAS, highlighting the importance of activation of the RAS-RAF-MEK-ERK-MAP kinase pathway in the progression of serrated neoplasms.

There is strong evidence in support of a pathway to colorectal carcinogenesis through serrated polyps: (a) morphological studies have reported evolution of HP to invasive carcinoma (sometimes through intermediate lesions of SA and HP/AD; Refs. 18, 19, 20, 21 ) and have shown that 11% of SAs harbor foci of intramucosal cancer (17) ; and (b) patients affected by the rare hyperplastic polyposis have an increased risk of colorectal cancer (33, 34, 35, 36, 37, 38) , and some of these polyps in fact manifest the morphology of SAs (39) .

The molecular basis of the serrated neoplasm–colorectal carcinoma sequence is currently poorly characterized. Previous studies have shown heterogeneity of genetic alterations in SAs, some suggesting a higher frequency of p53 mutation (25) , loss of heterozygosity (22) , MSI (23) , and CpG island methylator phenotype (40 , 41) in these lesions compared with HPs. However, the involvement of the RAS-RAF-MEK-ERK-MAP kinase pathway in the progression has been questioned. Despite the presence of KRAS mutations in 11–47% of HPs (22 , 26 , 29) , in SAs, most studies have reported a low incidence (5–18%; Refs. 22 , 30 , and 42 ), raising the possibility of an alternative mechanism for early evolution. Our finding of BRAF mutations in all of the SAs examined, therefore, serves to provide a missing link in the pathogenesis of serrated neoplasms. The data suggest that acquisition of a BRAF mutation is associated with the progression of HP to SA, whereas progression to HP/AD is predominantly associated with acquisition of a KRAS mutation.

MSI has been reported previously in serrated polyps. It has therefore been proposed that serrated polyps may be the precursors of microsatellite unstable/mismatch repair-deficient colorectal cancers (23 , 24 , 43) . Moreover, Rajagopalan et al. (5) have recently suggested that BRAF mutations are positively associated with MSI in colorectal cancer. These findings prompted us to examine MSI in our series of serrated polyps. Using three monomorphic microsatellite markers, we did not detect instability in any of the 69 serrated polyps studied. Taken together with our previous data (4) , we do not observe a relationship between MSI and BRAF mutations in colorectal epithelial neoplasms. The lack of MSI in our series of serrated polyps is not surprising, given the fact that only three of our HP/ADs are located in the right colon, and the monomorphic microsatellite markers predominantly detect those with high level MSI. Even in previous studies, high level MSI is uncommon in serrated polyps, and most is restricted to HP/ADs occurring in the proximal colon (23 , 41) .

The relative contributions of the serrated neoplasm–carcinoma sequence compared with the classical AD-carcinoma pathway in colorectal cancer development have been difficult to assess. Morphological studies have been of limited utility because serrated lesions are usually small and can easily be destroyed by overgrowth of the cancers that subsequently develop. Nevertheless, by identifying remnant SA elements at the edge of invasive colorectal cancers, it has been estimated that 6% of sporadic colorectal cancers originate from an SA (18) . Molecular studies have also yielded few insights because there have been previously no known molecular changes that specifically characterize the serrated neoplasm–carcinoma pathway. The high frequency of BRAF mutations in HP (30%) and SA (100%) reported here is in sharp contrast to the low incidence observed in classical ADs (2.8%; Ref. 4 ). We therefore propose that the group of colorectal cancers carrying BRAF mutations (estimated at between 5 to 10%) may have evolved, at least in part, from HP through the intermediate stage of SA. However, the high incidence of BRAF mutations in HPs and particularly SAs compared with that observed in colorectal cancer suggests that the majority of colorectal cancers do not evolve through this pathway. HPs that progress through HP/ADs predominantly have KRAS mutations. This makes the adenomatous components of HP/ADs indistinguishable from classical ADs both at the morphological and molecular levels. Hence, their contribution to colorectal cancer is more difficult to assess.

	ACKNOWLEDGMENTS

 
We thank the Genome Research Centre of the University of Hong Kong for their support.

	FOOTNOTES

 
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

¹ Supported by the Committee on Research and Conference Grant 10204404 from the University of Hong Kong, the Research Grants Council of the Hong Kong Special Administrative Region (HKU 7330/00M), and the Wellcome Trust.

² To whom requests for reprints should be addressed, at Department of Pathology, The University of Hong Kong, Queen Mary Hospital, Hong Kong. Phone: 852 28554401; Fax: 852 28725197; E-mail: suetyi{at}hkucc.hku.hk (S. Y. L.) or E-mail: styuen{at}hkucc.hku.hk (S. T. Y.).

³ The abbreviations used are: MEK, mitogen-activated protein/extracellular signal-regulated kinase kinase; MAP, mitogen-activated protein; ERK, extracellular signal-regulated kinase; HP, hyperplastic polyp; HP/AD, admixed hyperplastic polyp/adenoma; SA, serrated adenoma; MSI, microsatellite instability.

Received 3/25/03. Revised 5/ 6/03. Accepted 5/21/03.

	REFERENCES

Top ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 

1. Peyssonnaux C., Eychene A. The Raf/MEK/ERK pathway: new concepts of activation. Biol. Cell, 93: 53-62, 2001.[Medline]
2. Kolch W. Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions. Biochem. J., 351: 289-305, 2000.
3. Davies H., Bignell G. R., Cox C., Stephens P., Edkins S., Clegg S., Teague J., Woffendin H., Garnett M. J., Bottomley W., Davis N., Dicks E., Ewing R., Floyd Y., Gray K., Hall S., Hawes R., Hughes J., Kosmidou V., Menzies A., Mould C., Parker A., Stevens C., Watt S., Hooper S., Wilson R., Jayatilake H., Gusterson B. A., Cooper C., Shipley J., Hargrave D., Pritchard-Jones K., Maitland N., Chenevix-Trench G., Riggins G. J., Bigner D. D., Palmieri G., Cossu A., Flanagan A., Nicholson A., Ho J. W., Leung S. Y., Yuen S. T., Weber B. L., Seigler H. F., Darrow T. L., Paterson H., Marais R., Marshall C. J., Wooster R., Stratton M. R., Futreal P. A. Mutations of the BRAF gene in human cancer. Nature (Lond.), 417: 949-954, 2002.[Medline]
4. Yuen S. T., Davies H., Chan T. L., Ho J. W., Bignell G. R., Cox C., Stephens P., Edkins S., Tsui W. W., Chan A. S., Futreal P. A., Stratton M. R., Wooster R., Leung S. Y. Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia. Cancer Res., 62: 6451-6455, 2002.[Abstract/Free Full Text]
5. Rajagopalan H., Bardelli A., Lengauer C., Kinzler K. W., Vogelstein B., Velculescu V. E. Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status. Nature (Lond.), 418: 934 2002.[Medline]
6. Brose M. S., Volpe P., Feldman M., Kumar M., Rishi I., Gerrero R., Einhorn E., Herlyn M., Minna J., Nicholson A., Roth J. A., Albelda S. M., Davies H., Cox C., Brignell G., Stephens P., Futreal P. A., Wooster R., Stratton M. R., Weber B. L. BRAF and RAS mutations in human lung cancer and melanoma. Cancer Res., 62: 6997-7000, 2002.[Abstract/Free Full Text]
7. Naoki K., Chen T. H., Richards W. G., Sugarbaker D. J., Meyerson M. Missense mutations of the BRAF gene in human lung adenocarcinoma. Cancer Res., 62: 7001-7003, 2002.[Abstract/Free Full Text]
8. Pollock P. M., Harper U. L., Hansen K. S., Yudt L. M., Stark M., Robbins C. M., Moses T. Y., Hostetter G., Wagner U., Kakareka J., Salem G., Pohida T., Heenan P., Duray P., Kallioniemi O., Hayward N. K., Trent J. M., Meltzer P. S. High frequency of BRAF mutations in nevi. Nat. Genet., 33: 19-20, 2003.[Medline]
9. Fearon E. R., Vogelstein B. A genetic model for colorectal tumorigenesis. Cell, 61: 759-767, 1990.[Medline]
10. Vogelstein B., Fearon E. R., Hamilton S. R., Kern S. E., Preisinger A. C., Leppert M., Nakamura Y., White R., Smits A. M., Bos J. L. Genetic alterations during colorectal-tumor development. N. Engl. J. Med., 319: 525-532, 1988.[Abstract]
11. Hawkins N. J., Bariol C., Ward R. L. The serrated neoplasia pathway. Pathology, 34: 548-555, 2002.[Medline]
12. Jass J. R., Whitehall V. L., Young J., Leggett B. A. Emerging concepts in colorectal neoplasia. Gastroenterology, 123: 862-876, 2002.[Medline]
13. Lieberman D. A., Weiss D. G., Bond J. H., Ahnen D. J., Garewal H., Chejfec G. Use of colonoscopy to screen asymptomatic adults for colorectal cancer. Veterans Affairs Cooperative Study Group 380. N. Engl. J. Med., 343: 162-168, 2000.[Abstract/Free Full Text]
14. Imperiale T. F., Wagner D. R., Lin C. Y., Larkin G. N., Rogge J. D., Ransohoff D. F. Risk of advanced proximal neoplasms in asymptomatic adults according to the distal colorectal findings. N. Engl. J. Med., 343: 169-174, 2000.[Abstract/Free Full Text]
15. Tateyama H., Li W., Takahashi E., Miura Y., Sugiura H., Eimoto T. Apoptosis index and apoptosis-related antigen expression in serrated adenoma of the colorectum: the saw-toothed structure may be related to inhibition of apoptosis. Am. J. Surg. Pathol., 26: 249-256, 2002.[Medline]
16. Jass J. R. Serrated route to colorectal cancer: back street or super highway?. J. Pathol., 193: 283-285, 2001.[Medline]
17. Longacre T. A., Fenoglio-Preiser C. M. Mixed hyperplastic adenomatous polyps/serrated adenomas. A distinct form of colorectal neoplasia. Am. J. Surg. Pathol., 14: 524-537, 1990.[Medline]
18. Makinen M. J., George S. M., Jernvall P., Makela J., Vihko P., Karttunen T. J. Colorectal carcinoma associated with serrated adenoma–prevalence, histological features, and prognosis. J. Pathol., 193: 286-294, 2001.[Medline]
19. Tanaka M., Kusumi T., Sasaki Y., Yamagata K., Ichinohe H., Nishida J., Kudo H. Colonic intra-epithelial carcinoma occurring in a hyperplastic polyp via a serrated adenoma. Pathol. Int., 51: 215-220, 2001.[Medline]
20. Yao T., Nishiyama K., Oya M., Kouzuki T., Kajiwara M., Tsuneyoshi M. Multiple ‘serrated adenocarcinomas’ of the colon with a cell lineage common to metaplastic polyp and serrated adenoma. Case report of a new subtype of colonic adenocarcinoma with gastric differentiation. J. Pathol., 190: 444-449, 2000.[Medline]
21. Jass J. R., Cottier D. S., Pokos V., Parry S., Winship I. M. Mixed epithelial polyps in association with hereditary non-polyposis colorectal cancer providing an alternative pathway of cancer histogenesis. Pathology, 29: 28-33, 1997.[Medline]
22. Fogt F., Brien T., Brown C. A., Hartmann C. J., Zimmerman R. L., Odze R. D. Genetic alterations in serrated adenomas: comparison to conventional adenomas and hyperplastic polyps. Hum. Pathol., 33: 87-91, 2002.[Medline]
23. Iino H., Jass J. R., Simms L. A., Young J., Leggett B., Ajioka Y., Watanabe H. DNA microsatellite instability in hyperplastic polyps, serrated adenomas, and mixed polyps: a mild mutator pathway for colorectal cancer?. J. Clin. Pathol., 52: 5-9, 1999.[Abstract]
24. Hawkins N. J., Ward R. L. Sporadic colorectal cancers with microsatellite instability and their possible origin in hyperplastic polyps and serrated adenomas. J. Natl. Cancer Inst. (Bethesda), 93: 1307-1313, 2001.[Abstract/Free Full Text]
25. Hiyama T., Yokozaki H., Shimamoto F., Haruma K., Yasui W., Kajiyama G., Tahara E. Frequent p53 gene mutations in serrated adenomas of the colorectum. J. Pathol., 186: 131-139, 1998.[Medline]
26. Jen J., Powell S. M., Papadopoulos N., Smith K. J., Hamilton S. R., Vogelstein B., Kinzler K. W. Molecular determinants of dysplasia in colorectal lesions. Cancer Res., 54: 5523-5526, 1994.[Abstract/Free Full Text]
27. Bardi G., Pandis N., Fenger C., Kronborg O., Bomme L., Heim S. Deletion of 1p36 as a primary chromosomal aberration in intestinal tumorigenesis. Cancer Res., 53: 1895-1898, 1993.[Abstract/Free Full Text]
28. Lothe R. A., Andersen S. N., Hofstad B., Meling G. I., Peltomaki P., Heim S., Brogger A., Vatn M., Rognum T. O., Borresen A. L. Deletion of 1p loci and microsatellite instability in colorectal polyps. Genes Chromosomes Cancer, 14: 182-188, 1995.[Medline]
29. Otori K., Oda Y., Sugiyama K., Hasebe T., Mukai K., Fujii T., Tajiri H., Yoshida S., Fukushima S., Esumi H. High frequency of K-ras mutations in human colorectal hyperplastic polyps. Gut, 40: 660-663, 1997.[Abstract/Free Full Text]
30. Sawyer E. J., Cerar A., Hanby A. M., Gorman P., Arends M., Talbot I. C., Tomlinson I. P. Molecular characteristics of serrated adenomas of the colorectum. Gut, 51: 200-206, 2002.[Abstract/Free Full Text]
31. Dehari R. Infrequent APC mutations in serrated adenoma. Tohoku J. Exp. Med., 193: 181-186, 2001.
32. Chan T. L., Yuen S. T., Chung L. P., Ho J. W., Kwan K. Y., Chan A. S., Ho J. C., Leung S. Y., Wyllie A. H. Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer. J. Natl. Cancer Inst. (Bethesda), 91: 1221-1226, 1999.[Abstract/Free Full Text]
33. Bengoechea O., Martinez-Penuela J. M., Larrinaga B., Valerdi J., Borda F. Hyperplastic polyposis of the colorectum and adenocarcinoma in a 24-year-old man. Am. J. Surg. Pathol., 11: 323-327, 1987.[Medline]
34. Jeevaratnam P., Cottier D. S., Browett P. J., Van De Water N. S., Pokos V., Jass J. R. Familial giant hyperplastic polyposis predisposing to colorectal cancer: a new hereditary bowel cancer syndrome. J. Pathol., 179: 20-25, 1996.[Medline]
35. McCann B. G. A case of metaplastic polyposis of the colon associated with focal adenomatous change and metachronous adenocarcinomas. Histopathology, 13: 700-702, 1988.[Medline]
36. Teoh H. H., Delahunt B., Isbister W. H. Dysplastic and malignant areas in hyperplastic polyps of the large intestine. Pathology, 21: 138-142, 1989.[Medline]
37. Leggett B. A., Devereaux B., Biden K., Searle J., Young J., Jass J. Hyperplastic polyposis: association with colorectal cancer. Am. J. Surg. Pathol., 25: 177-184, 2001.[Medline]
38. Rashid A., Houlihan P. S., Booker S., Petersen G. M., Giardiello F. M., Hamilton S. R. Phenotypic and molecular characteristics of hyperplastic polyposis. Gastroenterology, 119: 323-332, 2000.[Medline]
39. Torlakovic E., Snover D. C. Serrated adenomatous polyposis in humans. Gastroenterology, 110: 748-755, 1996.[Medline]
40. Chan A. O., Issa J. P., Morris J. S., Hamilton S. R., Rashid A. Concordant CpG island methylation in hyperplastic polyposis. Am. J. Pathol., 160: 529-536, 2002.[Abstract/Free Full Text]
41. Park S. J., Rashid A., Lee J. H., Kim S. G., Hamilton S. R., Wu T. T. Frequent CpG island methylation in serrated adenomas of the colorectum. Am. J. Pathol., 162: 815-822, 2003.[Abstract/Free Full Text]
42. Ajioka Y., Watanabe H., Jass J. R., Yokota Y., Kobayashi M., Nishikura K. Infrequent K-ras codon 12 mutation in serrated adenomas of human colorectum. Gut, 42: 680-684, 1998.[Abstract/Free Full Text]
43. Jass J. R., Young J., Leggett B. A. Hyperplastic polyps and DNA microsatellite unstable cancers of the colorectum. Histopathology, 37: 295-301, 2000.[Medline]

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				S. Crawford, D. Belajic, J. Wei, J. P. Riley, P. J. Dunford, S. Bembenek, A. Fourie, J. P. Edwards, L. Karlsson, A. Brunmark, et al. A novel B-RAF inhibitor blocks interleukin-8 (IL-8) synthesis in human melanoma xenografts, revealing IL-8 as a potential pharmacodynamic biomarker Mol. Cancer Ther., March 1, 2008; 7(3): 492 - 499. [Abstract] [Full Text] [PDF]

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				J. Young and J. R. Jass The case for a genetic predisposition to serrated neoplasia in the colorectum: hypothesis and review of the literature. Cancer Epidemiol. Biomarkers Prev., October 1, 2006; 15(10): 1778 - 1784. [Abstract] [Full Text] [PDF]

				M. R. Sapio, D. Posca, G. Troncone, G. Pettinato, L. Palombini, G. Rossi, G. Fenzi, and M. Vitale Detection of BRAF mutation in thyroid papillary carcinomas by mutant allele-specific PCR amplification (MASA) Eur. J. Endocrinol., February 1, 2006; 154(2): 341 - 348. [Abstract] [Full Text] [PDF]

				K. Haigis, J. Sage, J. Glickman, S. Shafer, and T. Jacks The Related Retinoblastoma (pRb) and p130 Proteins Cooperate to Regulate Homeostasis in the Intestinal Epithelium J. Biol. Chem., January 6, 2006; 281(1): 638 - 647. [Abstract] [Full Text] [PDF]

				K. Sweet, J. Willis, X.-P. Zhou, C. Gallione, T. Sawada, P. Alhopuro, S. K. Khoo, A. Patocs, C. Martin, S. Bridgeman, et al. Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis JAMA, November 16, 2005; 294(19): 2465 - 2473. [Abstract] [Full Text] [PDF]

				I.-M. Shih and R. J. Kurman Molecular Pathogenesis of Ovarian Borderline Tumors: New Insights and Old Challenges Clin. Cancer Res., October 15, 2005; 11(20): 7273 - 7279. [Abstract] [Full Text] [PDF]

				C W Wong, Y S Fan, T L Chan, A S W Chan, L C Ho, T K F Ma, the Cancer Genome Project, S T Yuen, and S Y Leung BRAF and NRAS mutations are uncommon in melanomas arising in diverse internal organs J. Clin. Pathol., June 1, 2005; 58(6): 640 - 644. [Abstract] [Full Text] [PDF]

				R. Beach, A. O.-O. Chan, T.-T. Wu, J. A. White, J. S. Morris, S. Lunagomez, R. R. Broaddus, J.-P. J. Issa, S. R. Hamilton, and A. Rashid BRAF Mutations in Aberrant Crypt Foci and Hyperplastic Polyposis Am. J. Pathol., April 1, 2005; 166(4): 1069 - 1075. [Abstract] [Full Text] [PDF]

				A J M Watson Apoptosis and colorectal cancer Gut, November 1, 2004; 53(11): 1701 - 1709. [Full Text] [PDF]

				C.-L. Ho, R. J. Kurman, R. Dehari, T.-L. Wang, and I.-M. Shih Mutations of BRAF and KRAS Precede the Development of Ovarian Serous Borderline Tumors Cancer Res., October 1, 2004; 64(19): 6915 - 6918. [Abstract] [Full Text] [PDF]

				T Kambara, L A Simms, V L J Whitehall, K J Spring, C V A Wynter, M D Walsh, M A Barker, S Arnold, A McGivern, N Matsubara, et al. BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum Gut, August 1, 2004; 53(8): 1137 - 1144. [Abstract] [Full Text] [PDF]

				T Higuchi and J R Jass My approach to serrated polyps of the colorectum J. Clin. Pathol., July 1, 2004; 57(7): 682 - 686. [Abstract] [Full Text] [PDF]

				T. Ikenoue, Y. Hikiba, F. Kanai, J. Aragaki, Y. Tanaka, J. Imamura, T. Imamura, M. Ohta, H. Ijichi, K. Tateishi, et al. Different Effects of Point Mutations within the B-Raf Glycine-Rich Loop in Colorectal Tumors on Mitogen-Activated Protein/Extracellular Signal-Regulated Kinase Kinase/Extracellular Signal-Regulated Kinase and Nuclear Factor {kappa}B Pathway and Cellular Transformation Cancer Res., May 15, 2004; 64(10): 3428 - 3435. [Abstract] [Full Text] [PDF]

				K. Konishi, T. Yamochi, R. Makino, K. Kaneko, T. Yamamoto, H. Nozawa, A. Katagiri, H. Ito, K. Nakayama, H. Ota, et al. Molecular Differences between Sporadic Serrated and Conventional Colorectal Adenomas Clin. Cancer Res., May 1, 2004; 10(9): 3082 - 3090. [Abstract] [Full Text] [PDF]

				C V A Wynter, M D Walsh, T Higuchi, B A Leggett, J Young, and J R Jass Methylation patterns define two types of hyperplastic polyp associated with colorectal cancer Gut, April 1, 2004; 53(4): 573 - 580. [Abstract] [Full Text] [PDF]

				M. Xing, Y. Cohen, E. Mambo, G. Tallini, R. Udelsman, P. W. Ladenson, and D. Sidransky Early Occurrence of RASSF1A Hypermethylation and Its Mutual Exclusion with BRAF Mutation in Thyroid Tumorigenesis Cancer Res., March 1, 2004; 64(5): 1664 - 1668. [Abstract] [Full Text] [PDF]

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