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EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis



Ephrin receptor B2 (EPHB2) has recently been proposed as a novel tumor suppressor gene in colorectal cancer (CRC). Inactivation of the gene has been shown to correlate with progression of colorectal tumorigenesis, and somatic mutations have been reported in both colorectal and prostate tumors.


Here we have analyzed the EPHB2 gene for germline alterations in 101 individuals either with 1) CRC and a personal or family history of prostate cancer (PC), or 2) intestinal hyperplastic polyposis (HPP), a condition associated with malignant degeneration such as serrated adenoma and CRC.


Four previously unknown missense alterations were observed, which may be associated with the disease phenotype. Two of the changes, I361V and R568W, were identified in Finnish CRC patients, but not in over 300 Finnish familial CRC or PC patients or more than 200 population-matched healthy controls. The third change, D861N, was observed in a UK HPP patient, but not in additional 40 UK HPP patients or in 200 UK healthy controls. The fourth change R80H, originally identified in a Finnish CRC patient, was also found in 1/106 familial CRC patients and in 9/281 healthy controls and is likely to be a neutral polymorphism.


We detected novel germline EPHB2 alterations in patients with colorectal tumors. The results suggest a limited role for these EPHB2 variants in colon tumor predisposition. Further studies including functional analyses are needed to confirm this.

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The Wnt signaling pathway plays a central role in the development of colorectal cancer (CRC). In the majority of cases the early events in tumorigenesis involve inactivation of the tumor suppressor gene APC and stabilization of β-catenin [1, 2]. The constitutive activity of β-catenin/T cell factor-4 (Tcf-4) –complex leads to transcription of growth promoting genes, which together with subsequent inactivation of tumor suppressor genes drive the tumorigenesis further and enable the formation of abnormal growth patterns.

One of the direct transcriptional targets of β-catenin is Ephrin receptor B2 (EPHB2), whose protein product mediates the bi-directional migration and correct positioning of the cells along the crypt axis in the intestinal epithelium [3]. The gene is located in chromosomal region 1p36, which is frequently altered in many types of cancer [4]. Recent findings have demonstrated that EPHB2 appears to have a role in tumor progression, and acts as a tumor suppressor gene in colorectal cancer. In the study by Batlle et al. (2005) EPHB2 activity was observed to suppress CRC progression as the disruption of EphB2 in Apc min/+ mice was shown to accelerate tumor formation and growth in colon and rectum [5]. In addition, premalignant lesions of the colon were shown to express high levels of EPHB2, whereas the expression was reduced in more advanced tumor stages [5]. Somatic mutations in EPHB2 have been observed both in colorectal and prostate tumors, and an EPHB2 germline mutation has been associated with an increased prostate cancer (PC) risk [68]. Huusko et al. (2004) identified a nonsense mutation Q723X in a PC cell line, which led to the identification of other novel missense (R199H, A297S, D679N, T909M), nonsense (K1019X), frameshift and splice site mutations in prostate tumors obtained from patients in USA and Switzerland [7]. In a later study by Kittles et al. (2005) the nonsense mutation K1019X was found to increase risk for PC over two-fold in an African American hereditary PC sample set [8]. In 2005, Alazzouzi et al. observed frequent frameshift mutations on the A9 repeat of the EPHB2 gene in primary colorectal tumors in patients of mostly Caucasian origin (Finland, Germany, Spain and Japan) [6].

In our recent study we found decreased EPHB2 gene expression and protein levels in tumors with serrated CRC when compared to tumors from patients with conventional CRC [9]. While no somatic EPHB2 mutations were observed in the serrated CRC tumors, one patient was found to harbor a germline EPHB2 alteration. This, together with the growing evidence of the role of EPHB2 in CRC tumorigenesis, prompted us to further investigate the role of EPHB2 in colorectal tumor predisposition. In this study, we have analyzed the EPHB2 gene for germline alterations in 101 patients with either 1) CRC and personal or family history of PC or 2) hyperplastic polyposis (HPP), a condition believed to be associated with serrated CRC [10].


Patient material

Altogether 101 normal tissue samples were collected from medical institutions in Finland, UK and USA from patients with 1) CRC and either personal or family history of PC (n = 63, mean age of onset 69 years, range 30–85 years) or 2) hyperplastic polyposis (n = 38, mean age of onset 46 years, range 16–69) (Table 1). The CRC patients belong to a well characterized and previously described population based series of 1042 Finnish CRC patients [11, 12]. Family history of PC was considered positive if the patient had a first degree relative diagnosed with PC. HPP was diagnosed if there were at least three but typically over 10 histopathologically verified hyperplastic polyps. If less than five polyps were observed, at least two of them had to be large (>1.0 cm). The UK patients had between 10 to over 100 HPs, and the mean age of onset was 43 years (range 16–79 years). Five patients had one or more large HPs (range 1–3 cm), two had serrated adenomas, one had mixed adenomatous/hyperplastic polyps, three had adenomas and one had juvenile polyps. Family history of polyps or cancer was detected in 10% of these individuals, and 40% of these had developed CRC. Patients from the US had in general over 30 HPs, the mean age at HPP diagnosis was 51 years (range 19-68 years), and all but one had been diagnosed with serrated adenomas. In two cases there was history of HPP in the family. The two Finnish HPP patients were diagnosed with multiple hyperplastic polyps and serrated adenomas at 44 and 41 years of age.

Table 1 Selection criteria of the 101 patients screened for germline EPHB2 mutations.

The frequencies of the observed EPHB2 variants were further analyzed in either Finnish familial prostate (n = 164, mean age of onset 63 years, range 40–86 years) and colorectal (n = 159, mean age of onset 65 years, range 27–90 years) cancer patients, or in additional UK HPP patients (n = 40, mean age of onset 54 years, range 23–74), respectively. The Finnish CRC patients belong to the aforementioned population based series of CRC patients [11, 12]. The familial PC cohort has also been previously well characterized and described [13, 14]. In addition, 282 samples from anonymous Finnish blood donors and 200 healthy UK individuals served as population-matched controls, respectively.

Patient information and samples were collected after obtaining informed consent. The study was approved by the ethics review committee of the Hospital District of Helsinki and Uusimaa (Dnr. 133/E8/03).

Mutation analysis

Mutation screening of the EPHB2 gene [GenBank: AF025304] in the 101 normal tissue samples was performed by direct sequencing (ABI PRISM 3100 Genetic Analyzer, Applied Biosystems, Foster City, CA). All coding exons with at least 70 nucleotides intronic sequence at the exon-intron boundaries, except exon 1, were sequenced. Primer sequences and PCR conditions are available upon request. Loss of heterozygosity (LOH) was analyzed by comparing sequences from the normal and the corresponding tumor DNA at the site of a variant. Frequencies of the observed alterations in familial CRC, PC and HPP patient samples, as well as in healthy population-matched controls, were determined by either direct sequencing or DHPLC (variant R568W). The DHPLC analysis was performed using the Agilent 1100 Services DHPLC Instrumentation (Agilent, Palo Alto, CA) with HPLC Column 50 × 3.0 mm × ¼" Helix DNA (Varian, Palo Alto, CA), Helix BufferPak DNA Analysis buffers "A" and "B" (Varian), and the following parameters: T = 64°C, flow 0.4 ml/min, gradient 3 min 58–66% B-buffer.


Altogether four heterozygous germline missense changes, all previously unreported, were observed in the initial EPHB2 mutation screening of 101 samples (Table 2). An I361V (1081A>G) alteration in exon 5 was detected in a Finnish patient diagnosed with a microsatellite stable (MSS) rectal cancer at the age of 75 years and PC at the age of 73 years. The variant was not present in 164 familial PC patients, in 139 of 159 familial CRC patients (data from 87% of cases) or in 239 of 282 healthy population-matched controls (data from 85% of cases). The corresponding tumor tissue displayed loss of the wild type allele. This residue resides in the fibronectin type III domain, which is in the extracellular part of the protein and participates in cell-surface binding. Another missense change, R568W (1702C>T) in exon 9, was detected in a Finnish patient diagnosed with a MSS colon cancer at the age of 69 years. The patient's father, whose carrier status is unknown, had been diagnosed with PC at the age of 82 years. The variant was not observed in 164 familial PC patients, in 145 familial CRC patients (data from 91% of cases), or in 279 healthy Finnish controls. No loss of the wild type allele was observed in the colon tumor tissue. The residue is located in a juxtamembrane segment before a kinase domain in the intracellular part of the protein. The third missense alteration, D861N (2581G>A) in exon 14, was detected in a UK patient diagnosed with HPP at the age of 58 years. A review of her clinico-pathologic history revealed that, to date, she has had serrated adenomas and over 100 pancolonically distributed sessile HPs. The patient's mother, from whom no sample was available, had died of CRC at the age of 36 years. The variant was not observed in the additional 40 HPP patients or in 200 healthy UK controls. Due to the unavailability of tumor tissue DNA, LOH could not be determined. The variant is located in the intracellular protein kinase domain of EPHB2. The fourth change, R80H (239G>A) in exon 3, was initially observed in a Finnish patient whose MSS colon cancer was diagnosed at the age of 73 years. The patient's brother had been diagnosed with PC at the age of 60 years, and her father had died of gastric cancer at the age of 57 years. The variant was also found in 1/106 (0.9%) familial CRC patients and in 9/281 (3.2%) healthy population-matched controls. No loss of the wild type allele was observed in the tumor tissue. The variant is situated in the N-terminal ligand-binding domain at the extracellular part of the protein.

Table 2 Observed EPHB2 germline variations in colorectal cancer and hyperplastic polyposis patients.


Ephrin receptors constitute a large family of receptor protein tyrosine kinases that together with ephrins, their membrane-bound receptor-like ligands, participate in developmental processes requiring organized patterning and movement of cells, such as axonal guidance, signal transduction, cell morphogenesis and angiogenesis [15, 16]. These proteins are widely expressed in adult tissues with organ specific patterns [17]. In the intestine the most prominent ephrin receptor is EPHB2 [17]. Recently, the loss of EPHB2 expression has been associated with colorectal carcinogenesis. The reduction of the EPHB2 levels has been found to correlate with the degree of malignancy, as a significant decrease in number of EPHB2 positive cells and in staining intensity has been observed at the adenoma-carcinoma transition [5, 18, 19]. In our recent study, we found even more profound reduction in EPHB2 levels in colorectal tumors with serrated histology when compared to conventional CRC [9]. The link between reduced EPHB2 expression and poor survival has also been demonstrated [19]. In mouse studies, reduced Ephb2 activity has been shown to accelerate tumorigenesis in the colon and rectum, and to result in the formation of aggressive adenocarcinomas in Apc Min/+ mice [3]. Based on the growing evidence of the role of EPHB2 in CRC, we hypothesized that EPHB2 germline alterations may predispose to colorectal tumors.

We found a total of four previously unknown EPHB2 germline alterations, of which three may associate with the disease phenotype. The corresponding tumor DNA was available from two variant carriers, and one of the tumors displayed loss of the wild type allele. All three alterations are located in amino acids showing conservation across species from mouse, rat, chicken and cow down to fish, and were not observed in more than 200 healthy population-matched controls. However, the possibility that some or all of these variants are rare polymorphisms cannot be excluded, and further studies are needed to elucidate their functional significance.

In Finland, occurrence of recurrent founder mutations in several cancer susceptibility genes has been successfully utilized to evaluate the impact of these gene defects in extensive sets of patients and families [11, 12, 20]. Therefore, to further analyze the importance of the EPHB2 variants observed in the Finnish patients (I361V and R568W), their frequencies were analyzed among more than 300 Finnish familial CRC and PC patients. No additional carriers were observed. This suggests that the contribution of these rare germline alterations to familial CRC and PC burden in Finland is limited. The UK variant D861N was not observed in additional 40 HPP patients or in 200 healthy UK controls, suggesting as well a possible role for the variant in colorectal tumor susceptibility.

Overall, germline variants that may be associated with the disease phenotype were seen in 3/101 (3.0%) of patients analyzed for the EPHB2 gene. Our data are compatible with the results by Oba et al. (2001), who found no EPHB2 germline mutations among 50 CRC patients [21]. Therefore, although some possibly disease associated germline EPHB2 variants do exist and may play a role in colorectal tumor predisposition, the observed EPHB2 inactivation in CRCs is largely due to other mechanisms, such as promoter hypermethylation that has frequently been observed in both MSI and MSS tumors, LOH, and somatic mutations in a coding region repeat sequence in MSI colorectal tumors [6, 18].

While EPHB2 is the prominent ephrin receptor in the intestine [17], also other members of the protein family may have a role in colorectal tumorigenesis. For example, a dramatic 94-fold decrease in EPHA6 expression has been observed in colorectal tumors when compared to normal tissue, and EPHA8 expression has been detected only in colon tumor but not in corresponding normal tissue [17]. Furthermore, a pattern of inactivation similar to EPHB2 has been observed for EPHB4 and EPHB3 in colorectal tumors and/or cell lines, respectively [5]. Also somatic mutations in the kinase domain of EPHA3 have been identified in colorectal tumors [22]. Further studies are needed to more thoroughly elucidate the possible role of this large protein family in CRC tumorigenesis.


We report here the first EPHB2 germline alterations in patients with colorectal tumors. However, the rarity of such alterations in this and in a previous study [21], together with the sequential loss of EPHB2 expression during colorectal carcinogenesis, suggests a limited role for EPHB2 in CRC predisposition and speaks for the more pronounced role for EPHB2 in tumor progression than in tumor initiation. Notwithstanding, germline EPHB2 variants do exist and may be associated with colon tumor predisposition, but further studies including functional analyses are needed to confirm this.



colorectal cancer


gastric cancer


hyperplastic polyp


hyperplastic polyposis


ephrin receptor B2


denaturing high performance liquid chromatography


microsatellite stable


  1. Bienz M, Clevers H: Linking colorectal cancer to Wnt signaling. Cell. 2000, 103: 311-320. 10.1016/S0092-8674(00)00122-7.

    Article  CAS  PubMed  Google Scholar 

  2. Powell SM, Zilz N, Beazer-Barclay Y, Bryan TM, Hamilton SR, Thibodeau SN, Vogelstein B, Kinzler KW: APC mutations occur early during colorectal tumorigenesis. Nature. 1992, 359: 235-237. 10.1038/359235a0.

    Article  CAS  PubMed  Google Scholar 

  3. Batlle E, Henderson JT, Beghtel H, van den Born MM, Sancho E, Huls G, Meeldijk J, Robertson J, van de Wetering M, Pawson T, Clevers H: Beta-catenin and TCF mediate cell positioning in the intestinal epithelium by controlling the expression of EphB/ephrinB. Cell. 2002, 111: 251-263. 10.1016/S0092-8674(02)01015-2.

    Article  CAS  PubMed  Google Scholar 

  4. Sulman EP, Tang XX, Allen C, Biegel JA, Pleasure DE, Brodeur GM, Ikegaki N: ECK, a human EPH-related gene, maps to 1p36.1, a common region of alteration in human cancers. Genomics. 1997, 40: 371-374. 10.1006/geno.1996.4569.

    Article  CAS  PubMed  Google Scholar 

  5. Batlle E, Bacani J, Begthel H, Jonkheer S, Gregorieff A, van de Born M, Malats N, Sancho E, Boon E, Pawson T, Gallinger S, Pals S, Clevers H: EphB receptor activity suppresses colorectal cancer progression. Nature. 2005, 435: 1126-1130. 10.1038/nature03626.

    Article  CAS  PubMed  Google Scholar 

  6. Alazzouzi H, Davalos V, Kokko A, Domingo E, Woerner SM, Wilson AJ, Konrad L, Laiho P, Espin E, Armengol M, Imai K, Yamamoto H, Mariadason JM, Gebert JF, Aaltonen LA, Schwartz SJ, Arango D: Mechanisms of inactivation of the receptor tyrosine kinase EPHB2 in colorectal tumors. Cancer Res. 2005, 65: 10170-10173. 10.1158/0008-5472.CAN-05-2580.

    Article  CAS  PubMed  Google Scholar 

  7. Huusko P, Ponciano-Jackson D, Wolf M, Kiefer JA, Azorsa DO, Tuzmen S, Weaver D, Robbins C, Moses T, Allinen M, Hautaniemi S, Chen Y, Elkahloun A, Basik M, Bova GS, Bubendorf L, Lugli A, Sauter G, Schleutker J, Ozcelik H, Elowe S, Pawson T, Trent JM, Carpten JD, Kallioniemi OP, Mousses S: Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer. Nat Genet. 2004, 36: 979-983. 10.1038/ng1408.

    Article  CAS  PubMed  Google Scholar 

  8. Kittles RA, Boffoe-Bonnie A, Moses T, Robbins C, Ahaghotu C, Huusko P, Pettaway C, Vijayakumar S, Bennett J, Hoke G, Mason T, Weinrich S, Trent J, Collins F, Mousses S, Bailey-Wilson J, Furbert-Harris P, Dunston G, Powell I, Carpten JD: A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history. J Med Genet. 2005

    Google Scholar 

  9. Laiho P., Kokko A., Vanharanta S., Salovaara R., Sammalkorpi H., Järvinen H., Mecklin JP., Karttunen TJ., Tuppurainen K., Davalos V., Schwartz Jr S., Arango D., Mäkinen MJ., LA. A: Serrated carcinomas form a subclass of colorectal cancer with distinct molecular basis. Oncogene.

  10. Makinen MJ, George SM, Jernvall P, Makela J, Vihko P, Karttunen TJ: Colorectal carcinoma associated with serrated adenoma--prevalence, histological features, and prognosis. J Pathol. 2001, 193: 286-294. 10.1002/1096-9896(2000)9999:9999<::AID-PATH800>3.0.CO;2-2.

    Article  CAS  PubMed  Google Scholar 

  11. Aaltonen LA, Salovaara R, Kristo P, Canzian F, Hemminki A, Peltomaki P, Chadwick RB, Kaariainen H, Eskelinen M, Jarvinen H, Mecklin JP, de la Chapelle A: Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med. 1998, 338: 1481-1487. 10.1056/NEJM199805213382101.

    Article  CAS  PubMed  Google Scholar 

  12. Salovaara R, Loukola A, Kristo P, Kaariainen H, Ahtola H, Eskelinen M, Harkonen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Jarvinen H, Mecklin JP, Aaltonen LA, de la Chapelle A: Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol. 2000, 18: 2193-2200.

    CAS  PubMed  Google Scholar 

  13. Seppala EH, Ikonen T, Autio V, Rokman A, Mononen N, Matikainen MP, Tammela TL, Schleutker J: Germ-line alterations in MSR1 gene and prostate cancer risk. Clin Cancer Res. 2003, 9: 5252-5256.

    PubMed  Google Scholar 

  14. Schleutker J, Matikainen M, Smith J, Koivisto P, Baffoe-Bonnie A, Kainu T, Gillanders E, Sankila R, Pukkala E, Carpten J, Stephan D, Tammela T, Brownstein M, Bailey-Wilson J, Trent J, Kallioniemi OP: A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease. Clin Cancer Res. 2000, 6: 4810-4815.

    CAS  PubMed  Google Scholar 

  15. Kullander K, Klein R: Mechanisms and functions of Eph and ephrin signalling. Nat Rev Mol Cell Biol. 2002, 3: 475-486. 10.1038/nrm856.

    Article  CAS  PubMed  Google Scholar 

  16. Pasquale EB: Eph receptor signalling casts a wide net on cell behaviour. Nat Rev Mol Cell Biol. 2005, 6: 462-475. 10.1038/nrm1662.

    Article  CAS  PubMed  Google Scholar 

  17. Hafner C, Schmitz G, Meyer S, Bataille F, Hau P, Langmann T, Dietmaier W, Landthaler M, Vogt T: Differential gene expression of Eph receptors and ephrins in benign human tissues and cancers. Clin Chem. 2004, 50: 490-499. 10.1373/clinchem.2003.026849.

    Article  CAS  PubMed  Google Scholar 

  18. Guo DL, Zhang J, Yuen ST, Tsui WY, Chan AS, Ho C, Ji J, Leung SY, Chen X: Reduced expression of EphB2 that parallels invasion and metastasis in colorectal tumors. Carcinogenesis. 2006, 27: 454-464. 10.1093/carcin/bgi259.

    Article  CAS  PubMed  Google Scholar 

  19. Lugli A, Spichtin H, Maurer R, Mirlacher M, Kiefer J, Huusko P, Azorsa D, Terracciano L, Sauter G, Kallioniemi OP, Mousses S, Tornillo L: EphB2 expression across 138 human tumor types in a tissue microarray: high levels of expression in gastrointestinal cancers. Clin Cancer Res. 2005, 11: 6450-6458. 10.1158/1078-0432.CCR-04-2458.

    Article  CAS  PubMed  Google Scholar 

  20. Syrjakoski K, Vahteristo P, Eerola H, Tamminen A, Kivinummi K, Sarantaus L, Holli K, Blomqvist C, Kallioniemi OP, Kainu T, Nevanlinna H: Population-based study of BRCA1 and BRCA2 mutations in 1035 unselected Finnish breast cancer patients. J Natl Cancer Inst. 2000, 92: 1529-1531. 10.1093/jnci/92.18.1529.

    Article  CAS  PubMed  Google Scholar 

  21. Oba SM, Wang YJ, Song JP, Li ZY, Kobayashi K, Tsugane S, Hamada GS, Tanaka M, Sugimura H: Genomic structure and loss of heterozygosity of EPHB2 in colorectal cancer. Cancer Lett. 2001, 164: 97-104. 10.1016/S0304-3835(00)00716-3.

    Article  CAS  PubMed  Google Scholar 

  22. Bardelli A, Parsons DW, Silliman N, Ptak J, Szabo S, Saha S, Markowitz S, Willson JK, Parmigiani G, Kinzler KW, Vogelstein B, Velculescu VE: Mutational analysis of the tyrosine kinome in colorectal cancers. Science. 2003, 300: 949-10.1126/science.1082596.

    Article  CAS  PubMed  Google Scholar 

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We would like to thank Sini Marttinen and Iina Vuoristo for assistance. The study was supported by grants from the European Commission (QLG2-CT-2001-01861), Finnish Cancer Society, the Academy of Finland (212901), Sigrid Juselius Foundation, Finnish Cultural Foundation, The Research and Science Foundation of Farmos and Foundation for Technological Advancement. This work was carried out at the Center of Excellence in Translational Genome-Scale Biology of the Academy of Finland. CE is a recipient of the Doris Duke Distinguished Clinical Scientist Award.

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Correspondence to Lauri A Aaltonen.

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AK, PL, RL, SK and LGCC carried out the genetic studies. AK, PV and LAA were responsible for drafting and revising the manuscript. LAA, HJ, J-PM, IPMT, JS and CE were involved in design of the study, providing important intellectual content and acquisition of the study material. All authors read and approved the final manuscript.

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Kokko, A., Laiho, P., Lehtonen, R. et al. EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis. BMC Cancer 6, 145 (2006).

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