Open Access

Polymorphisms of the ICAM-1 exon 6 (E469K) are associated with differentiation of colorectal cancer

  • Qing-lei Wang1,
  • Bing-hui Li2Email author,
  • Bin Liu1,
  • Ya-bin Liu2,
  • Yue-Ping Liu2,
  • Sui-Bing Miao1,
  • Yi Han1,
  • Jin-Kun Wen1 and
  • Mei Han1
Journal of Experimental & Clinical Cancer Research200928:139

https://doi.org/10.1186/1756-9966-28-139

Received: 29 July 2009

Accepted: 13 October 2009

Published: 13 October 2009

Abstract

Background

Genetic factors are thought to play a role in development for colorectal carcinogenesis. ICAM-1 is a polymorphic gene, thus, the present study investigated the relationship between the polymorphisms of ICAM-1 and the susceptibility and phenotypical characteristics of colorectal cancer (CRC).

Methods

The polymorphisms at ICAM-1 exon 4 (G241R) and exon 6 (E469K) were detected by PCR with sequence-specific primers. The relationship between specific genotypes of ICAM-1 and differentiation of CRC was evaluated by the histological grade.

Results

We showed only GG genotype of ICAM-1 individuals in either CRC or normal controls. The KK genotype of ICAM-1 K469E was found more frequently than in the controls (P < 0.05). Patients with well-differentiated CRC displayed the KK more frequently than those of poor differentiation (P < 0.05).

Conclusion

The findings indicate that polymorphisms of G241R are rare in Chinese population and that KK genotype of ICAM-1 K469E is significantly associated with well differentiation of CRC.

Background

Colorectal cancer (CRC) is a common malignant disease around the world. CRC has an extremely poor prognosis owing to insidious symptomatology, late clinical presentation and rapid progression and so lead to poor 5-year disease-free survival [1, 2]. CRC is related not only to living habits such as dietary but also to the susceptibility of heredity [3]. Individuals who have first-degree relative with CRC have the increased risk of the CRC compared with those without a family history [4], suggesting that genetic factors contribute to risk for colorectal carcinogenesis [5].

The intercellular adhesion molecule-1 (ICAM-1) is a single-chain cell surface glycoprotein that belongs to the immunoglobulin superfamily. It is known that ICAM-1 can be aberrantly expressed in CRC and suppress cancer progression via activation of the host immune surveillance system and prevention of cells from detaching from the primary tumor mass and thus attenuate or eliminate metastasis [6, 7]. Two single-base polymorphisms in human ICAM-1 gene have been reported, in exon 4 and 6, changing codons 241(G241R) and 469(K469E), respectively, which are common genetic variations associated with diseases [8]. However, it is not well documented that the association of the ICAM-1 gene polymorphisms with CRC development. In present study, we analyze the association between the polymorphisms at exon 4 (G241R) and exon 6 (E469K) of ICAM-1 and CRC susceptibility and in vivo differences in ICAM-1 level and differentiation in tumor tissues of patients with CRC. Our results suggest that tumor cell differentiation may be influenced by genetic variation in ICAM-1 in Chinese population.

Materials and methods

Study population

87 cases were patients with a new diagnosis of colorectal adenocarcinoma attending a Hebei Medical University Forth Hospital, China between December 2007 and August 2008. 102 volunteers without CRC were used as controls. The average age of the subjects was 55 years (range, 34-83 years). The peripheral blood specimens from patients with CRC and controls were collected at the time of the diagnosis after informed consent was obtained. All the tumor and matched normal tissues investigated in this study were obtained from patients who had undergone a surgical resection. The diagnosis and staging of CRC were assessed according to the WHO classifications [9] and TMN classifications [10]. The study was approved by the institutional research board at Hebei Medical University.

Genotyping of ICAM-1 gene polymorphisms

Genomic DNA was extracted and purified from whole blood lymphocytes using a blood DNA Kit (Omega Bio-Tek Co., USA) according to the manufacturer's instructions. PCR with sequence-specific primers (SSP) was used to detect the ICAM-1 polymorphisms at Exon 4 (G241R) and Exon 6 (E469K) as described elsewhere [11, 12]. For G241R in exon 4, two sequence-specific forward primers: 5'-GTGGTCTGTTCCCTGGACG-3'(G241) and 5'-GTGGTCTGTTCCCTGGACA-3' (R241), and for K469E (exon 6) two sequence-specific reverse primers: 5'-GCACATTCACGGTCACCTC-3' (K469) and 5'-GCACATTCACGGTCACCTT-3' (E469) were used. Each combination of the four primers contained one forward primer and one reverse primer for the 927 bp fragment of sequence-specific amplifications, respectively. For the positive internal control, the primers 5'-GAAGGTGAAGGTCGGAGT-3'(forward) and 5'-GAAGATGGTGATGGGATTTC-3' (reverse) coding for the 225 bp fragment of human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene were used.

PCR was performed in a final volume of 20 μl in 96-well plates. The final concentrations of the reagents were as follows: 200 μM of each dNTP, 2.5 mM MgCl2, 0.5 μM of each primer, polymerase buffer, between 0.01 and 0.1 mg DNA, and 0.2 units of Taq polymerase (Promaga). The PCR cycle conditions were 94°C for 4 min, followed by 35 cycles at 94°C for 30 s, 69°C for 45 s and 72°C for 40 s, with a final extension step at 72°C for 10 min. 927 bp of PCR product was identified by gel electrophoresis on 2% agarose gels stained with ethidium bromide.

ICAM-1 expression analysis

Western blot analysis was used to detect ICAM-1 protein expression in both tumor and matched adjacent normal tissues from patient with CRC as described previously [13]. The tissue lysates were prepared from the colorectal tissues [14]. Equal amounts of proteins were separated by electrophoresis on an 8% SDS-polyacrylamide gel and then electrophorytically transferred to polyvinylidene difluoride membranes (Millipore Co, Billerica, Massachusetts, USA). The membrane was incubated with anti-ICAM-1 antibody (1:1000; Santa Cruz), followed by a secondary anti-rabbit antibody (1:20000; Santa Cruz) using chemiluminescence protocol (Santa Cruz).

Immunohistochemistry analysis

Immunostaining of sections from CRC tissues was performed with the anti-ICAM-1 (1:200) as described previously [15]. Staining intensities were determined by measuring the integrated optical density (IOD) with light microscopy using a computer-based Image-Pro Morphometric System by two independent observers in a double-blind manner.

Statistical analysis

Each polymorphism was tested in controls to ensure the fitting with Hardy-Weinberg equilibrium. To test the hypothesis of association between genetic polymorphisms and CRC, multivariate methods based on logistic regression analyses were used. Allele and genotype frequencies in all subjects were calculated by direct counting. Hardy-Weinberg equilibrium was tested using the Fisher's exact test. The strength of the gene-cancer associations was measured by odds ratio (OR) and its 95% confidence interval (CI). P < 0.05 was considered statistically significant. The SPSS was used in the statistical analysis.

Results

Polymorphism of ICAM-1 K469 E may be associated with CRC risk

The polymorphisms of ICAM-1 in all cases and controls are shown in Table 1, which were conformed to Hardy-Weinberg equilibrium (P > 0.05). In either CRC cases or controls, only GG genotype of ICAM-1 exon 4 (G241R) was identified, while the exon 6 (K469E) homozygous and heterozygous individuals were observed (Figure 1). The distribution of the ICAM-1 K469E genotypes was significantly different between CRC cases and controls (P < 0.05). In 102 controls, the K allele frequency was 63.73%, which is different from that in the cancer cases (73.56%). Subjects with K allele in CRC had a 1.58-fold increase, compared with controls (P = 0.041). K allele was significantly associated with a increased risk of CRC (OR = 1.58, χ2 = 4.194, 95% CI, 1.02~2.46, P = 0.041). The frequency of KK genotype in CRC cases was more than that in the controls (57.47% vs 42.16%, χ2 = 4.406, P = 0.036). Subjects with KK genotype had a 1.85-fold increase in CRC risk compared with those with KE+EE genotypes.
Table 1

Allele and genotype frequencies of the ICAM-1 K469E polymorphisms in CRC cases and controls

 

CRC (n = 87) (%)

Controls (n = 102) (%)

P

OR (95% CI)

Genotype

    

   KK

50 (57.47)

43 (42.16)

  

   KE

28 (32.18)

44 (43.14)

0.036a

1.85 (1.04~3.31)b

   EE

9 (10.35)

15 (14.7)

  

Allele

    

K

E

128 (73.56)

46 (26.44)

130 (63.73)

74 (36.27)

0.041

1.58 (1.02~2.46)c

OR, odds ratio; CI, confidence interval.

a, Genotypes: KK vs KE+EE.

b, OR for KK vs KE+EE genotypes in CRC.

c, OR for K vs E allele in CRC.

Figure 1

ICAM-1 G241R and K469E genotypes. Lane M: Marker; Primers: G241-E469 (lane 1,5,9); G241-K469(lane 2,6,10); R241-E469(lane 3,7,11); R241-K469 (lane 4,8,12).

Polymorphism of ICAM-1 K469E is associated with tumor differentiation

The potential associations of the ICAM-1 K469E genotype with tumor characteristics are presented in Table 2. No correlation was found between K469E genotypes and tumor location, presence of lymph node metastases, Dukes stage, or age and gender at diagnosis. The KK genotype was more frequently found in cases with a well-differentiated CRC (P = 0.033) (Figure 2A and Table 2), although with the increased CRC risk. In contrast, the tumor tissues from the cases with KE+EE genotype showed poor differentiation compared with those with KK genotype (P < 0.05). The results suggest that there is correlation between the K469E genotype and the phenotypical characteristics of CRC.
Table 2

Distribution of various genotypes of ICAM-1 K469E in relation to clinicopathological and other variables in CRC cases

Variables

Cases (n)

KK

KE+EE

χ 2

P

Age

     

   ≤ 55

27

16

11

0.051

0.821

   > 55

60

34

26

  

Gender

     

   Male

49

28

21

0.005

0.944

   Female

38

22

16

  

Tumor location

     

   Colon

30

14

16

0.004

0.95

   Rectum

57

27

30

  

Differentiation

     

Well and moderately

62

33

29

4.564

0.033

Poorly

25

7

18

  

Metastasis

     

   No

75

41

34

1.75

0.186

   Yes

12

9

3

  

Dukes stages

     

   A+B

50

30

20

0.308

0.579

   C+D

37

20

17

  
Figure 2

Polymorphism of ICAM-1 K469E is associated with cancer differentiation and ICAM-1 expression in CRC. (A), Representative histological sections of CRC with KK and EE genotypes (Magnification, × 400); (B), Western blot analysis for ICAM-1 expression of CRC with KK, KE and EE genotypes; (C), Densitometric scanning of Western blots, n = 15, * P < 0.05 vs controls; # P < 0.05 vs CRC with KK genotype; (D), Representative ICAM-1 staining of the cross sections of CRC with KK, KE and EE genotypes (Magnification, × 400); (E), Average IOD of ICAM-1 staining of CRC cross sections (n = 15). IOD represents relative ICAM-1 protein level in tumor tissues. * P < 0.05 vs KE+EE genotypes.

KK genotype is correlated with increase in ICAM-1 expression in tumor tissues

We next set out to assess whether the K469E genotype is correlated with differences in ICAM-1 expression using lysate extracted from the tumor and matched adjacent normal tissues of CRC patients with KK or KE+EE genotypes. There were no differences in ICAM-1 level in matched normal tissues of all tested patients. KK genotype patients showed an increase in the expression of ICAM-1 protein in tumor tissues relative to the matched normal tissues (P < 0.05, Figure 2B and 2C). However, the difference of ICAM-1 level between tumor and matched normal tissues was not observed in the patients with KE+EE genotypes. Meanwhile, ICAM-1 level was higher in the tumor tissues of individuals with KK genotype than that of the KE+EE genotypes (P < 0.05). We also observed that the distribution of ICAM-1 was exclusively extracellular in all colorectal tumors (Figure 2D and 2E). Taken together, these results indicate that ICAM-1 protein is accumulated in CRC tissues with KK genotype.

Discussion

Polymorphisms of ICAM-1 K469E and G241R are common genetic variation in populations and associated with several autoimmune diseases, such as multiple sclerosis, type 1 diabetes, or Crohn's disease [12, 16, 17]. In current study, we have found only GG genotype individuals in either CRC cases or normal controls. The variants in G241R were not observed in our tested population, suggesting that the polymorphisms of G241R may be rare in Chinese, consistent with the Japanese and Koreans, respectively, probably reflecting that there is a common ancestor in these populations [16]. Our observation is different from the previous study concerning the G allele frequency in European-American population that showed less G allele frequency (0.796-0.971) [12, 18, 19]. The distribution of K469E genotypes and allele frequencies in exon 6 of the ICAM-1 was significantly different between CRC patients and controls, and between patients with well differentiation and poor differentiation of tumor tissues. In CRC patients, the KK genotype was found more frequently than in the controls. The previous studies have shown that the K allele frequency is 0.437-0.630 in different populations [16, 20]. The KK genotype frequency in patients with well-differentiated tumor tissues was more than that in those of poor differentiation. Although the significance and the functional or therapeutic relevance of our findings remain to be elucidated, the most important finding is that the poor prognosis of CRC seems to be associated with allele E.

Although it is unclear how the ICAM-1 K469E polymorphism contributes to the pathogenesis of CRC, we found that the increase in ICAM-1 expression was accompanied by well-differentiation in tumor tissues of KK genotype patients. ICAM-1, as a surface glycoprotein, is expressed on vascular endothelium, macrophages, and activated lymphocytes, and mediates leukocyte circulation and extravasation from the blood into the areas of inflammation and macrophage differentiation [2123]. The epithelial cells of adult colon do not normally express ICAM-1 which can be expressed subsequent to malignant transformation [24, 25]. ICAM-1 expression decreases CRC metastasis and suppress cancer progression via promoting tumor cell motility and attachment to the extracellular matrix [6]. The previous study has showed that expression level of ICAM-1 is high in well differentiated tumor cells and low levels in poorly differentiated cells, and demonstrated a mechanism whereby ICAM-1 expression promotes CRC differentiation and retard metastasis [7]. ICAM-1 plays a role in promoting lymphocyte-mediated tumor killing [26], and this occurs as a result of enhanced binding of peripheral blood mononuclear cells to the tumor cells and subsequent tumor cell lysis [27]. Yet the study suggests that ICAM-1 enhances tumor cell attachment to the extracellular matrix by promoting motility in the context of remodeling, and appears to be acting as a morphogen [7]. These findings provide a possible reason why increasing of ICAM-1 expression occurs in well differentiated CRC tissues.

Conclusion

Our study herein provides a potential genetic factor for the differentiation of CRC that correlates with ICAM-1 K469E polymorphisms because of different ICAM-1 expression. However, we are unable to define the association of the ICAM-1 K469E polymorphisms with CRC risk owing to the limitations of the size of the CRC and control populations in the present study. Our findings may help to evaluate the prognosis of CRC according to the individual genetic background.

Declarations

Acknowledgements

The subject was supported by grants from National Natural Science Foundation of the People's Republic of China (No. 30973820) and the Hebei Province Science and Technology Plan Programs of the People's Republic of China (No. 09276406D).

Authors’ Affiliations

(1)
Department of Biochemistry and Molecular Biology, Institute of Basic Medicine, Hebei Medical University
(2)
Department of Surgery, Fourth Hospital, Hebei Medical University

References

  1. Bahl R, Arora S, Nath N, Mathur M, Shukla NK, Ralhan R: Novel polymorphism in p21(waf1/cip1) cyclin dependent kinase inhibitor gene: association with human esophageal cancer. Oncogene. 2000, 19: 323-328. 10.1038/sj.onc.1203325.View ArticleGoogle Scholar
  2. Klintrup K, Makinen JM, Kauppila S, Vare PO, Melkko J, Tuominen H, Tuppurainen K, Makela J, Karttunen TJ, Makinen MJ: Inflammation and prognosis in colorectal cancer. Eur J Cancer. 2005, 41: 2645-2654. 10.1016/j.ejca.2005.07.017.View ArticleGoogle Scholar
  3. Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, Koskenvuo M, Pukkala E, Skytthe A, Hemminki K: Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med. 2000, 343: 78-85. 10.1056/NEJM200007133430201.View ArticleGoogle Scholar
  4. Johns LE, Houlston RS: A systematic review and meta-analysis of familial colorectal cancer risk. Am J Gastroenterol. 2001, 96: 2992-3003. 10.1111/j.1572-0241.2001.04677.x.View ArticleGoogle Scholar
  5. Berndt SI, Platz EA, Fallin MD, Thuita LW, Hoffman SC, Helzlsouer KJ: Genetic variation in the nucleotide excision repair pathway and colorectal cancer risk. Cancer Epidemiol Biomarkers Prev. 2006, 15: 2263-2269. 10.1158/1055-9965.EPI-06-0449.View ArticleGoogle Scholar
  6. Alexiou D, Karayiannakis AJ, Syrigos KN, Zbar A, Kremmyda A, Bramis I, Tsigris C: Serum levels of E-selectin, ICAM-1 and VCAM-1 in colorectal cancer patients: correlations with clinicopathological features, patient survival and tumour surgery. Eur J Cancer. 2001, 37: 2392-2397. 10.1016/S0959-8049(01)00318-5.View ArticleGoogle Scholar
  7. Taglia L, Matusiak D, Matkowskyj KA, Benya RV: Gastrin-releasing peptide mediates its morphogenic properties in human colon cancer by upregulating intracellular adhesion protein-1 (ICAM-1) via focal adhesion kinase. Am J Physiol Gastrointest Liver Physiol. 2007, 292: G182-190. 10.1152/ajpgi.00201.2006.View ArticleGoogle Scholar
  8. Vora DK, Rosenbloom CL, Beaudet AL, Cottingham RW: Polymorphisms and linkage analysis for ICAM-1 and the selectin gene cluster. Genomics. 1994, 21: 473-477. 10.1006/geno.1994.1303.View ArticleGoogle Scholar
  9. Hamilton SRAL: World Health Organization classification of tumours. Pathology and genetics of tumors of digestive system. 2000, Lyon: IARC PressGoogle Scholar
  10. Greene FLPD, Fleming ID: The AJCC cancer staging manual. 2002, NewYork: Springer-Verlag, sixthView ArticleGoogle Scholar
  11. Gbadegesin RA, Watson CJ, Cotton SA, Brenchley PE, Webb NJ: A PCR-RFLP typing method for adhesion molecule gene polymorphisms and allele frequencies in a normal UK population. Eur J Immunogenet. 2002, 29: 109-111. 10.1046/j.1365-2370.2002.00277.x.View ArticleGoogle Scholar
  12. Braun C, Zahn R, Martin K, Albert E, Folwaczny C: Polymorphisms of the ICAM-1 gene are associated with inflammatory bowel disease, regardless of the p-ANCA status. Clin Immunol. 2001, 101: 357-360. 10.1006/clim.2001.5118.View ArticleGoogle Scholar
  13. Han M, Li AY, Meng F, Dong LH, Zheng B, Hu HJ, Nie L, Wen JK: Synergistic co-operation of signal transducer and activator of transcription 5B with activator protein 1 in angiotensin II-induced angiotensinogen gene activation in vascular smooth muscle cells. Febs J. 2009, 276: 1720-1728. 10.1111/j.1742-4658.2009.06902.x.View ArticleGoogle Scholar
  14. Liu B, Han M, Wen JK: Acetylbritannilactone Inhibits Neointimal Hyperplasia after Balloon Injury of Rat Artery by Suppressing Nuclear Factor-{kappa}B Activation. J Pharmacol Exp Ther. 2008, 324: 292-298. 10.1124/jpet.107.127407.View ArticleGoogle Scholar
  15. Fishbein MC, Wang T, Matijasevic M, Hong L, Apple FS: Myocardial tissue troponins T and I. An immunohistochemical study in experimental models of myocardial ischemia. Cardiovasc Pathol. 2003, 12: 65-71. 10.1016/S1054-8807(02)00188-6.View ArticleGoogle Scholar
  16. Nishimura M, Obayashi H, Maruya E, Ohta M, Tegoshi H, Fukui M, Hasegawa G, Shigeta H, Kitagawa Y, Nakano K, et al: Association between type 1 diabetes age-at-onset and intercellular adhesion molecule-1 (ICAM-1) gene polymorphism. Hum Immunol. 2000, 61: 507-510. 10.1016/S0198-8859(00)00101-4.View ArticleGoogle Scholar
  17. Killestein J, Schrijver HM, Crusius JB, Perez C, Uitdehaag BM, Pena AS, Polman CH: Intracellular adhesion molecule-1 polymorphisms and genetic susceptibility to multiple sclerosis: additional data and meta-analysis. Ann Neurol. 2000, 47: 277-279. 10.1002/1531-8249(200002)47:2<277::AID-ANA29>3.0.CO;2-Y.View ArticleGoogle Scholar
  18. Yang H, Vora DK, Targan SR, Toyoda H, Beaudet AL, Rotter JI: Intercellular adhesion molecule 1 gene associations with immunologic subsets of inflammatory bowel disease. Gastroenterology. 1995, 109: 440-448. 10.1016/0016-5085(95)90331-3.View ArticleGoogle Scholar
  19. Kretowski A, Wawrusiewicz N, Mironczuk K, Mysliwiec J, Kretowska M, Kinalska I: Intercellular adhesion molecule 1 gene polymorphisms in Graves' disease. J Clin Endocrinol Metab. 2003, 88: 4945-4949. 10.1210/jc.2003-030131.View ArticleGoogle Scholar
  20. Borozdenkova S, Smith J, Marshall S, Yacoub M, Rose M: Identification of ICAM-1 polymorphism that is associated with protection from transplant associated vasculopathy after cardiac transplantation. Hum Immunol. 2001, 62: 247-255. 10.1016/S0198-8859(01)00208-7.View ArticleGoogle Scholar
  21. Diamond MS, Staunton DE, Marlin SD, Springer TA: Binding of the integrin Mac-1 (CD11b/CD18) to the third immunoglobulin-like domain of ICAM-1 (CD54) and its regulation by glycosylation. Cell. 1991, 65: 961-971. 10.1016/0092-8674(91)90548-D.View ArticleGoogle Scholar
  22. Salmaso C, Olive D, Pesce G, Bagnasco M: Costimulatory molecules and autoimmune thyroid diseases. Autoimmunity. 2002, 35: 159-167. 10.1080/08916930290013441.View ArticleGoogle Scholar
  23. Bertry-Coussot L, Lucas B, Danel C, Halbwachs-Mecarelli L, Bach JF, Chatenoud L, Lemarchand P: Long-term reversal of established autoimmunity upon transient blockade of the LFA-1/intercellular adhesion molecule-1 pathway. J Immunol. 2002, 168: 3641-3648.View ArticleGoogle Scholar
  24. Dippold W, Wittig B, Schwaeble W, Mayet W, Meyer zum Buschenfelde KH: Expression of intercellular adhesion molecule 1 (ICAM-1, CD54) in colonic epithelial cells. Gut. 1993, 34: 1593-1597. 10.1136/gut.34.11.1593.View ArticleGoogle Scholar
  25. Kelly CP, O'Keane JC, Orellana J, Schroy PC, Yang S, LaMont JT, Brady HR: Human colon cancer cells express ICAM-1 in vivo and support LFA-1-dependent lymphocyte adhesion in vitro. Am J Physiol. 1992, 263: G864-870.Google Scholar
  26. Vanky F, Wang P, Patarroyo M, Klein E: Expression of the adhesion molecule ICAM-1 and major histocompatibility complex class I antigens on human tumor cells is required for their interaction with autologous lymphocytes in vitro. Cancer Immunol Immunother. 1990, 31: 19-27. 10.1007/BF01742491.View ArticleGoogle Scholar
  27. Tachimori A, Yamada N, Sakate Y, Yashiro M, Maeda K, Ohira M, Nishino H, Hirakawa K: Up regulation of ICAM-1 gene expression inhibits tumour growth and liver metastasis in colorectal carcinoma. Eur J Cancer. 2005, 41: 1802-1810. 10.1016/j.ejca.2005.04.036.View ArticleGoogle Scholar

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