Cyclin D1 and Rb protein expression and their correlation with prognosis in patients with colon cancer
© Kouraklis et al; licensee BioMed Central Ltd. 2006
Received: 23 August 2005
Accepted: 20 January 2006
Published: 20 January 2006
Cyclin D1 plays a major role as a potential contributor to the multistep process of oncogenesis; nevertheless its prognostic significance in colon cancer has already been examined in a few studies and needs to be further delineated. The aim of this study was to assess the expression of cyclin D1 and pRb and to correlate them with tumor histological stage and grade, proliferative capacity (Ki-67 labeling index) and clinical parameters, in order to delineate their impact on prognosis.
One hundred and eleven patients, who underwent surgical resection of the colon for colon cancer constituted the group of our study. The immunohistochemical expression of cyclin D1, Rb and Ki-67 proteins was examined and correlated with clinico-pathological parameters and survival.
The 5-years survival rate of patients presenting cyclin D1 positive tumors was 54%, while that of cyclin D1 negative ones was 67% (P = > 0.05). The survival rate of patients with pRb positive tumors was similar to that of pRb negatine ones. Significant association was observed between Ki-67 and cyclin D1 positivity (P = 0.045). Univariate analysis revealed worse survival in advanced stage patients presenting cyclin D1 positive tumors (P = 0.025). Additionally, the survival of patients aging less than 70 years old was correlated to cyclin D1 positivity (P = 0.009). Multivariate survival analysis revealed statistical significance for stage and hepatic metastasis.
Even though cyclin D1 and pRb have not disclosed any clear association with shorter survival, cyclin D1 positivity may be a useful predictor of subgroup patients with colon cancer being in advanced stage and early age.
In colon cancer patients, histological stage has been considered as the most important predictor of recurrence. However, for better management of patients, especially those within the same stage, additional factors should be examined. The product of the retinoblastoma gene (pRb) is the master regulator of entry into the cell- cycle in normal cells being deregulated in almost all tumors [1, 2]. The pRb activity is regulated by D-type cyclins and can be downmodulated by kinase inhibitors. The discovery of cyclins and their associated catalytic subunits, the cyclin dependent kinases (cdks), as key regulators of the cell-cycle progression, opened up a new debate on their possible involvement in tumorigenesis [1–3]. Recently has been demonstrated that cyclin D1 acts as an oncogene in vitro and in vivo . Once cells have entered the cell-cycle they are normally committed to go on and divide, hence the so called G1 cyclins have a predominant role in pushing cells toward progression. The cyclin D1/cdk4, cyclin D1/cdk6 and cyclin E/cdk2 complexes are the main regulators of the G1→S transition, each of them controlling a different and discrete rate limited step [2, 5, 6]. Among these, cyclin D1 presents the strongest evidence of a potential contribution to the multistep process of oncogenesis . However, limited number of studies have examined the association of cyclin D1 expression and prognosis of patients with different malignant tumors [8–12], while others have evaluated it in colon adenocarcinoma with equivocal results [13–16]. According to the previously published studies the role of cyclin D1 remains controversial with studies to report both positive and negative prognostic values since the role of cyclin D1 is complex and multiple.
In the present study, cyclin D1 and pRb expression was assessed immunohistochemically in tumoral tissues obtained from colon adenocarcinoma patients. Cyclin D1 and pRb immunohistochemical data were correlated with tumor histological stage and grade, proliferative capacity (Ki-67 labeling index), and clinical parameters, in order to delineate their impact on prognosis.
Patients and methods
One hundred and eleven consecutive patients, who underwent colonic surgical resection due to colon cancer constituted the group of our study (age range, 42–94; mean 70.6 years). Patients with unresectable colon cancer were excluded. Rectal cancer was also excluded from our study as most reports suggest that the survival of rectal cancer patients is poorer than that observed in colon cancer ones. Additionally, survival rate diminishes as rectal tumors are located more distally in the bowel. Sixty six of the patients were men (59.4%) and 45 (40.6%) were women. No patient received chemotherapy or radiation therapy before surgery. Surgical treatment was curative in all patients. Adjuvant chemotherapy was given in patients when the serosa was infiltrated by the tumor. Tumors were located in the cecum and the ascending colon in 31 cases (27.9%), in the transverse in 7 (6.3%), in the descending colon in 11 (9.9%) and in the sigmoid in 62 ones (55.9%). The resected tumors were histologically staged according to Dukes classification as: A, 16 cases (14.4%); B, 44 (39.6%); C, 26 (23.4%); and D, 25 (22.5%). Three levels of differentiation were used to classify grading as: well differentiated, 8 cases (7.2%); moderately, 83 (74.8%); and poorly, 20 (18%). The patients were followed for a time interval of 2 up to 68 months, mean 38.3 ± 16.7 months, median 38 months. Patients who were died during two months after surgery were excluded from the study, avoiding with this way deaths due to postoperative complications.
A mouse (IgG1 k) monoclonal antibody that reacts with human cyclin D1 (Santa Cruz Biochemicals, Santa Cruz, Calif., USA), a rabbit polyclonal one that reacts with human pRb (Santa Cruz Biochemicals), and another mouse (IgG1 k) monoclonal antibody (MIB-1) that reacts with Ki-67 antigen (Dakopatts, Glostrup, Denmark) were used in this study. Formalin-fixed paraffin-embedded tissue sections of 5 μm thickness were dewaxed in xylene and were brought to water through graded alcohols. Antigen retrieval was performed for Ki-67 antigen detection only, by microwaving slides in 10 mM citrate buffer (pH 6.0) for 15 min at high power, according to the manufacturer's instructions. To remove the endogenous peroxidase activity, sections were treated with freshly prepared 0.3% (vol/vol) hydrogen peroxide in methanol in dark, for 30 min, at room temperature (RT). Non-specific antibody binding was then blocked with a ready to use blocking reagent (Snipper, Biocare Biochemicals, Walnut Creek, CA, USA), for 10 min. The sections were then incubated for 1 h, at RT, with the primary antibodies diluted 1:100 in phosphate buffered saline (PBS). After washing three times with PBS, sections were incubated for 20 min at RT with linking biotinylated reagent, rabbit anti-mouse immunoglobulins (Dakopatts) for cyclin D1 and Ki-67 detection, and swine, anti-rabbit immunoglobulins for pRb one, both diluted 1:200 in PBS. The slides were then rinsed three times with PBS followed by incubation with peroxidase-conjugated streptavidin label (AB Complex, Dakopatts) for 20 min, at RT. Peroxidase activity was developed in 0.5% (vol/vol) 3,3'-diaminobenzidine hydrochloride (DAB, Sigma, Saint Louis, MO, USA) in PBS containing 0.03% (vol/vol) hydrogen peroxide for 2 min. Sections were counterstained with Harris' hematoxylin and mounted in gelatin (Sigma).
The stained sections were independently assessed by two different observers and specimens were considered "positive either for cyclin D1 or pRb" when more than 5% of tumor cells within the section were positively stained. Five percent was used as the cutoff value as referred in other studies [13, 15, 17]. The pattern of cyclin D1 and pRb immunostaining in positive cases was characterized either as nuclear only, or cytoplasmic and nuclear or cytoplasmic only. The intensity of cyclin D1 immunostaining in tumor cells was also semiquantitatively assessed as low (+), moderate (++), or high (+++). Control slides included in each experiment consisted of specific tissues previously shown to express the antigen of interest as positive controls (i.e. tonsil for cyclin D1 and pRb; normal colon for Ki-67). Internal experimental negative controls were also included by omission of the primary antibody. The fraction of Ki-67 positive cells was evaluated using a four graded scale of 0–5%, 6–25%, 26–50%, and >50%. Intraobserver discrepancies (<10%) were restained and reevaluated, and agreement was reached.
Statistical analysis was performed using the statistical package SPSS version 10.00. The correlation between cyclin D1, pRb and Ki-67 expression and various clinico-pathological variables (age, location, stage and grade, lymph node and liver metastasis and venous invasion) was assessed using the chi-square test. The Mann-Whitney U test was also applied in order to compare the correlation between Cyclin D1, pRB and Ki-67 expression in the colon cancer cases of our study. Survival curves were constructed using the Kaplan-Meier method and compared using the log rank test. The influence of each potential prognostic factor on the patients' survival was evaluated using Cox regression analysis. Results were considered statistically significant when P-value was less than 0.05.
Cyclin D1 and pRb expression in relation to different clinico-pathological characteristics (X2)
No of cases
Cyclin D1 expression
A and B
C and D
Well + Moderate
Lymph node metastas
Seventy one patients presented positive staining for pRb did not show any statistical significant association with clinico-pathological variables, as age, tumor location, histologic grade and stage, lymph node or hepatic metastasis, and vessel invasion (Table 1). The only pattern of immunostaining observed in pRb positive cases was the nuclear one. The intensity of pRb staining was assessed as low in 30 out of 71 cases (42.2%), as moderate in 20 out of 71 (28.2%), and as high in 21 out of 71 (29.6%). The survival rate of patients with pRb positive tumors was similar to that of pRb negative ones (data not shown). Among the 40 cases of pRb negative stained tumors, 18 of them were cyclin D1 negative. pRb expression was not statistically significantly associated with that of cyclin D1. The pattern of cyclin D1 immunostaining was not significantly associated with pRb expression (unpublished data).
Immunohistochemical expression of pRb and Ki-67 in relation to cyclin D1 expression.
No of cases
Cox proportional hazard model for factors associated with survival of colon cancer.
AB vs CD
Well+moderate vs. poor
Proximal vs. distal
Lymph node metastasis
Negative vs. positive
Negative vs. positive
Negative vs. positive
Yes vs. No
Negative vs. positive
Negative vs positive
In the present study, the expression of cyclin D1 and pRb in 111 cases of resected primary human colon carcinomas was investigated. The frequency of cyclin D1 positivity revealed in colon carcinoma cases was 63,9%, being similar to the results described by Arber et al , and higher than that reported by Palmqvist et al . In other studies, neither the pattern nor the intensity of cyclin D1 staining was scored. Differences in the pattern of cyclin D1 staining were noted in the colon cancer cases examined in our study. The presence of cytoplasmic pattern could suggest that not only elevated cyclin D1 levels occurring in colon cancer tumoral cells but alterations in the transport of the protein in the nucleus also exist. Due to the variety of parameters used, (e.g. antibodies, tissue fixation, threshold definitions for positivity or overexpression, semiquantitative scales), it is often difficult to make a direct comparison between the results obtained in different studies.
We have also reported lack of correlation between cyclin D1 and pRb positivity and clinico-pathological tumor characteristics. Positive cyclin D1 and pRb stainings did not show any specificity to the location of the tumor. Our results contrast with those of other studies that showed strong specificity to the right colon [13, 18], emphasizing the possibility that cancers developed in the right colon have a different spectrum of genetic damage and biological behavior than those developed in the left colon and rectum.
In our study, the proliferate activity (Ki-67 protein expression) in colon cancer cases was correlated with cyclin D1 levels (P = 0.045, Table 2) suggesting that cyclin D1 contributes to an increased proliferate potential that might be adequate in colon cancer cases . On the contrary, opposite results have been reported in breast , and hypopharyngeal  cancer. Thus, cyclin D1 might be important in the mechanisms behind malignancies, and it confers growth advantage, according to the obvious function in the G1-S transition.
It has been shown that cyclin D1 expression correlated with poor survival rate in a variety of human malignancies [8–10]. Previous studies have proposed a link between cyclin D1 expression and short survival rate in colon cancer patients [13, 15], while this correlation was not observed in three other published series [14, 16, 22, 23]. In the present study, only the survival of patients with cyclin D1 positive and advanced tumor stage (stage C and D) was significantly worse (P = 0.025). Our study also revealed that the survival rate of patients aged less than 70 years old presenting cyclin D1 positivity was significantly worse (P = 0.009), suggesting possibly that environmental effects are likely to dominate over genetic ones in older patients . This hypothesis has been reinforced recently by the study of Lichtenstein et al .
In our study of 111 colon cancer cases, the detection of pRb positivity has not disclosed a clear association with poor survival (P = 0.444). Regarding cyclin D1 positivity, our data indicate an association with shorter survival. We found a very significant correlation between Dukes' stage and poor clinical survival (P = 0.000). However, as in the clinical practice, the histological staging and differentiation provide the predominant prognostic information; it is therefore relevant to evaluate the relative contributions of cyclin D1 and pRb expression as compared to the clinico-pathological features. This evaluation can be performed by forward analysis in a Cox model . In such analysis, we did not find any statistical significance, or a higher relative risk factor of poor prognosis for pRb and cyclin D1 positivity within the same confidence interval. Our results are in agreement with those of others [13, 27] who also did not found any significant correlation.
The frequency of pRb positivity was 63.9%, and it was substantially more frequent than its inactivation. The frequency of pRb expression is in agreement with earlier observations that approximately one-third of colorectal cancers have increased copy numbers of one Rb1 allele [28, 29], a 2- to 5- fold increase in Rb protein and mRNA levels compared with adjacent normal mucosa , as well as a 2-fold increase of the abundance of pRb and its phosphorylation status compared with normal mucosa . It is known that the Rb gene is a tumor suppressor one and it is difficult to explain its overexpression in colon cancer. Presumably, it cannot be excluded that the Rb gene might contain genetic abnormalities which could lead to a functional inactivated protein with a subsequent longer degradation resulting in high protein levels [28, 32].
In conclusion, our study did not demonstrate an overall significantly worse prognosis in patients with cyclin D1 or pRb positivity. However, it showed that the survival rate of a patients subgroup presenting in advanced stage, or in patients aged less than 70 years old with cyclin D1 positive tumors was significantly worse. Consequently, our study indicates that cyclin D1 expression may be a predictor of patients presenting in advanced stage and of patients at young age. Thus, the importance of cyclin D1 expression seems to be complex and different between tumors, and therefore, our study encourage further and larger studies for cyclin D1 expression in colon cancer, in order to verify if the expression of this molecule indicates poor prognosis.
- Sherr CJ: Cancer cell cycle. Science. 1996, 274: 1672-1677. 10.1126/science.274.5293.1672.View ArticlePubMedGoogle Scholar
- Hartwell LH, Kastan MB: Cell cycle control and cancer. Science. 1994, 266: 1821-1828.View ArticlePubMedGoogle Scholar
- Otori K, Sugiyama K, Fukushima S, Esumi H: Expression of the cyclin D1 gene in rat colorectal aberrant crypt foci and tumors induced by azoxymethane. Cancer Letters. 1999, 140: 99-104. 10.1016/S0304-3835(99)00058-0.View ArticlePubMedGoogle Scholar
- Kazanov D, Shapira I, Pick M, Kolker O, Liberman E, Deutsch V: Oncogenic transformation of normal enterocytes by overexpression of cyclin D1. Dig Dis Sci. 2003, 48: 1251-1261. 10.1023/A:1024138605802.View ArticlePubMedGoogle Scholar
- Resnitzky D, Reed SI: Different roles for cyclins D1 and E in regulation of the G1 to S transition. Mol Cell Biol. 1995, 15: 3463-3469.PubMed CentralView ArticlePubMedGoogle Scholar
- Yu B, Lane ME, Pestell RG, Albanese S, Wadler S: Downregulation of cyclin D1 alters cdk-4 and cdk-2 specific phosphorylation of retinoblastoma protein. Mol Cell Biol Res Commun. 2000, 3: 352-359. 10.1006/mcbr.2000.0238.View ArticlePubMedGoogle Scholar
- Bartkova J, Lukas J, Strauss M, Bartek J: The Prad-1/cyclin D1 oncogene product accumulates aberrantly in a subset of colorectal carcinomas. Int J Cancer. 1994, 58: 568-573.View ArticlePubMedGoogle Scholar
- Naitoh H, Shibata J, Awaguchi A, Kodama M, Hattori T: Overexpression and localization of cyclin D1 mRNA and antigen in esophageal cancer. Am J Pathol. 1995, 146: 1161-1169.PubMed CentralPubMedGoogle Scholar
- Michalides R, Van Veelen N, Hart A, Loftus B, Wientjens E, Balm A: Overexpression of cyclin D1 correlates with recurrence in a group of forty seven operable squamus cell carcinomas of the head and neck. Cancer Res. 1995, 55: 975-978.PubMedGoogle Scholar
- Michalides R, Hageman P, Van Tinteren H: A clinico-pathological study on overexpression of cyclin D1 and of p53 in a series of 248 patients with operable breast cancer. Br J Cancer. 1996, 73: 728-734.PubMed CentralView ArticlePubMedGoogle Scholar
- Stendahl M, Kronbladt A, Ryden L, Emdin S, Benstsson NO, Landberg G: Cyclin D1 overexpression is a negative predictive factor for tamoxifen response in postmenopausal breast cancer patients. Br J Cancer. 2004, 90: 1942-1948. 10.1038/sj.bjc.6601831.PubMed CentralView ArticlePubMedGoogle Scholar
- van Diest PJ, Michalides RJ, Jannink L, van derValk P, Peterse HL, de Joug JS, Meijer CJ, Baak JP: Cyclin D1 expression in invasive breast cancer. Correlations and prognostic value. Am J Pathol. 1997, 150: 705-711.PubMed CentralPubMedGoogle Scholar
- Palmqvist R, Stenling R, Oberg A, Landberg G: Expression of cyclin D1 and retinoblastoma protein in colorectal cancer. Eur J Cancer. 1998, 34: 1575-1581. 10.1016/S0959-8049(98)00162-2.View ArticlePubMedGoogle Scholar
- Arber N, Hibshoosh H, Moss SF: Increased expression of cyclin D1 is an early event in multistage colorectal carcinogenesis. Gastroenterology. 1996, 110: 669-674. 10.1053/gast.1996.v110.pm8608874.View ArticlePubMedGoogle Scholar
- Maeda K, Chung YS, Kang SM: Cyclin D1 overexpression and prognosis in colorectal adenocarcinoma. Oncology. 1998, 55: 145-151. 10.1159/000011849.View ArticlePubMedGoogle Scholar
- Bondi J, Bukholm G, Nesland JM, Bukholm IR: Expression of non-membranous beta-catenin and gamma-catenin, c-Myc and cyclin D1 in relation to patient outcome in human colon adenocarcinomas. APMIS. 2004, 112: 49-56. 10.1111/j.1600-0463.2004.apm1120109.x.View ArticlePubMedGoogle Scholar
- McKay JA, Douglas JJ, Ross VG: Analysis of key cell-cycle checkpoint proteins in colorectal tumours. J Pathol. 2002, 196: 386-393. 10.1002/path.1053.View ArticlePubMedGoogle Scholar
- Holt PR, Mokoulu AD, Distler P, Liu T, Reddy BS: Regional distribution of carcinogen-induced colonic neoplasia in the rat. Nutr Cancer. 1996, 25: 129-135.View ArticlePubMedGoogle Scholar
- Callender T, El Naggar AK, Lee MS, Frankenthaler R, Luna MA, Batsakis JG: PRAD-1 (CCND1/cyclin D1 oncogene amplification in primary head and neck squamus cell carcinoma. Cancer. 1994, 74: 152-158.View ArticlePubMedGoogle Scholar
- Nielsen NH, Emdin SO, Cajander J, Landberg G: Deregulation of cyclin E and D1 in breast cancer is associated with inactivation of the retinoblastoma protein. Oncogene. 1997, 14: 295-304. 10.1038/sj.onc.1200833.View ArticlePubMedGoogle Scholar
- Masuda M, Hirakawa N, Nakashima T, Kuratomi Y, Komiyama S: Cyclin D1 overexpression in primary hypopharyngeal carcinomas. Cancer. 1996, 78: 390-395. 10.1002/(SICI)1097-0142(19960801)78:3<390::AID-CNCR2>3.0.CO;2-O.View ArticlePubMedGoogle Scholar
- Bukholm IK, Nesland JM: Protein expression of p53, p21 (WAF1/CIP1), bcl-2, Bax, cyclin D1 and pRb in human colon carcinomas. Virchows Arch. 2000, 436: 224-228. 10.1007/s004280050034.View ArticlePubMedGoogle Scholar
- Holland TA, Elder J, McCloud JM: Subcellular localization of cyclin D1 protein in colorectal; tumours is associated with p21 expression and correlates with patient survival. Int J Cancer. 2001, 95: 302-308. 10.1002/1097-0215(20010920)95:5<302::AID-IJC1052>3.0.CO;2-#.View ArticlePubMedGoogle Scholar
- Kong S, Wei Q, Amos CI: Cyclin D1 polymorphism and increased risk of colorectal cancer at young age. J Natl Cancer Inst. 2001, 93: 1106-1108. 10.1093/jnci/93.14.1106.View ArticlePubMedGoogle Scholar
- Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, Koskenvuo M: 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 ArticlePubMedGoogle Scholar
- Cox DR: Regression models and life tables. J R Stat Soc B. 1973, 31: 1333-1335.Google Scholar
- McKay JA, Douglas JJ, Ross VG: Expression of cell cycle control proteins in primary colorectal tumors does not always predict expression in lymph node metastases. Clin Cancer Res. 2000, 6: 1113-1118.PubMedGoogle Scholar
- Gope R, Christiansen MA, Thorson A: Increased expression of the retinoblastoma gene in human colorectal carcinomas ralative to normal colonic mucosa. J Natl Cancer Inst. 1990, 82: 310-314.View ArticlePubMedGoogle Scholar
- Meling GI, Lothe RA, Borresen AL: Genetic alterations within the retinoblastoma locus in colorectal carcinomas. Relation to DNA ploidy pattern studied by flow cytometric analysis. Br J Cancer. 1991, 64: 474-480.Google Scholar
- Gope R, Christensen MA, Thorson A: Molecular analysis of retinoblastoma gene in human colorectal carcinomas. Hereditary Colorectal Cancer. Edited by: Utsunomiya J, Lynch, HT. 1990, Tokyo Springer, 489-496.View ArticleGoogle Scholar
- Gope R, Gope ML: Abundance and state of phosphorylation of the retinoblastoma susceptibility gene product in human colon cancer. Mol Cell Biochem. 1992, 110: 123-133.View ArticlePubMedGoogle Scholar
- Yamamoto H, Soh Jae-Won, Monden T: Paradoxical increase in retinoblastoma protein in colorectal carcinomas may protect cells from apoptosis. Clin Cancer Res. 1999, 5: 1805-15.PubMedGoogle Scholar
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