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Regular Articles |
From the Divisions of Pathology*
and Medical
Oncology A,
Centro di Riferimento Oncologico,
Istituto di Ricovero e Cura a Carattere Scientifico, Istituto
Nazionale Tumori, Aviano, Italy; the Laboratory of
Virology,
Istituto Superiore di Sanità,
Roma, Italy; the Division of Medical Oncology,§
Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville,
Tennessee; and the Division of Internal Medicine,¶
Department of Medical Sciences, "Amedeo Avogadro" University of
Eastern Piedmont, Novara, Italy
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Abstract |
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 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
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Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The molecular pathogenesis of PEL is understood only in part. Most genetic lesions commonly seen in mature B-cell malignancies, eg, rearrangements of MYC, BCL-2, and BCL-6 as well as mutations of p531 (see Reference 2 for a review), are not involved in PEL pathogenesis. Conversely, it is conceivable that HHV-8 plays a pathogenetic role, because the virus encodes several genes which are homologous to cellular loci implicated in B-cell growth and survival3 (see review in Reference 4). One such gene is represented by the HHV-8 viral- (v-)cyclin that displays highest sequence similarity to the cellular D-type cyclins,4 a group of positive cell-cycle regulators that favor G1 progression. Although the precise function of v-cyclin is not fully known, it is conceivable that it shares several properties with cellular D-type cyclins. The expression of HHV-8 v-cyclin in latently infected PEL cells5 suggests a possible role of this molecule in growth control of the lymphoma.
The cellular D-type cyclins contribute to cell cycle control by forming complexes with catalytic subunits termed cyclin-dependent kinases (CDK).6,7 The activation of the CDK/cyclin complex is controlled by CDK inhibitors, which regulate cell cycle.7 A major inhibitor of the CDK/cyclins complex is represented by p27Kip1, a nuclear phosphoprotein belonging to the Kip family of CDK inhibitors.8-12 In physiological conditions, expression of p27Kip1 is highest in quiescent cells and declines as cells reenter the cell cycle. In lymphoid tissues, p27Kip1 is expressed in nonproliferating lymphocytes, whereas activated lymphocytes, eg, germinal center cells, score consistently negative for p27Kip1 expression.13 The inverse relationship between p27Kip1 expression and proliferation physiologically observed in normal lymphoid tissues is also encountered in most subtypes of NHL.13-15
The aims of the present study were: 1) to establish the expression pattern of p27Kip1 in PELs; and 2) to address the relationship between p27Kip1 expression, proliferation index, and expression of cellular cyclin D1 and v-cyclin of the lymphoma. We report that PELs consistently express p27Kip1 protein despite the high proliferative rate of the lymphoma clone, suggesting that p27Kip1 may be unable to drive cell-cycle arrest in PEL cells. Expression of p27Kip1 in PEL associates with expression of HHV-8 v-cyclin, but not of cellular cyclin D1, suggesting implications for PEL pathogenesis and growth. The co-existence of p27Kip1 expression and high proliferative index is a selective feature of PEL among lymphomas involving the serous body cavities, because secondary lymphomatous effusions generally display the inverse relationship between p27Kip1 positivity and growth fraction observed in most other types of NHL.
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Materials and Methods |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The present study was based on 18 samples of PEL and, for comparative purposes, 10 samples of HHV-8-negative lymphomatous effusions secondary to systemic B-cell NHL.
Samples of PEL included nine clinical tumor samples and nine cell
lines. Clinical samples were collected under sterile conditions during
routine diagnostic procedures at diagnosis; after centrifugation, the
effusion sediments were used to prepare cytospins and cell blocks. For
morphological study, cytospins were routinely fixed and stained by the
Papanicolaou method. For cell-block preparation, cell pellets were
Bouin- or formalin-fixed and treated according to a standard regimen
used at the Division of Pathology at Centro di Riferimento
Oncologico. The sectioned material from cell blocks was stained
with hematoxylin and eosin. In all cases the cytospins and cell blocks
prepared from fluid samples showed a tumor cell population 
95% as
evaluated by morphological and immunophenotypic analysis. Clinical
tumor samples were classified as PELs based on HHV-8 infection of the
tumor clone, and on specific morphological, immunophenotypic, and
molecular features, according to previously reported
criteria.1,2
Tumor cells usually exhibited an
indeterminate (non-B, non-T) phenotype (8 out of 9), lacked expression
of surface immunoglobulins and common B-cell associated antigens, were
devoid of rearrangements of the c-MYC gene, and clinically
displayed exclusive or predominant involvement of the serous body
cavities. Tumor cells from six PEL clinical samples carried
Epstein-Barr virus (EBV) infection, whereas tumor cells from the
remaining cases were EBV-negative. All, but one, PEL clinical samples
were obtained from patients infected with the human immunodeficiency
virus (HIV); the remaining sample was derived from an HIV-negative
individual.
The PEL cell lines included in this study were HBL-6, BC-1, BC-2, CRO-AP/2, CRO-AP/3, CRO-AP/5, BCBL-1, BC-3, and BCP-1.16-22 The detailed characterization of these cell lines has been reported previously16-22 (see review in Ref. 23 ). BCBL-1 was obtained through the AIDS Research and Reference Reagent Program, Division of AIDS, National Institute of Allergy and Infectious Diseases, National Institutes of Health. Five PEL cell lines (HBL-6, BC-1, BC-2, CRO-AP/2, and CRO-AP/5) carry EBV infection, whereas four PEL cell lines (BC-3, CRO-AP/3, BCBL-1, and BCP-1) are EBV-negative. All but two (BC-3 and BCP-1) PEL cell lines were derived from HIV-infected patients; BC-3 and BCP-1 were derived from HIV-negative individuals. All cell lines were cultured in RPMI 1640 (Life Technologies, Inc., Paisley, Scotland), supplemented with 10% heat-inactivated fetal bovine serum (Life Technologies, Inc.), 2 mmol/L L-glutamine (Life Technologies, Inc.), 100 U/ml penicillin, and 100 µg/ml streptomycin (Irvine Scientific, Santa Ana, CA) at 37°C in the presence of 5% CO2.
Secondary lymphomatous effusions, which were included in the study for comparative purposes, were collected and subjected to diagnostic procedures as described above. All secondary lymphomatous effusions scored negative for HHV-8 sequences, expressed B-cell markers and were assigned to the B-cell lineage. Clinically, all these effusions were documented at diagnosis. They were consistently associated with solid lymphomatous masses and were considered to be secondary to a tissue-based lymphoma (eight diffuse large B-cell lymphomas –B-DLCL - and two Burkitt’s lymphomas -BL). Tumor cells from two secondary lymphomatous effusions carried EBV infection, whereas tumor cells from the remaining cases were EBV-negative. All cases were included in a previous study.24 Three samples of secondary lymphomatous effusions were derived from HIV-infected individuals and seven were derived from HIV-negative individuals.
Immunocytochemistry
All cases had been immunophenotyped as previously described.20,22-24 Immunostaining was performed by using the avidin biotin peroxidase complex (ABC) method25 or by the alkaline phosphatase–anti-alkaline phosphatase method.26
The expression of p27Kip1 was investigated with the monoclonal antibody (mAb) Kip-1 (Transduction Laboratories, Lexington, KY). The proliferation index was assessed using the MIB-1 mAb (Immunotech, Marseille, France) directed against the Ki-67 nuclear proliferation antigen. Cellular cyclin D1 was assessed by using mAb AM29 (Zymed Laboratories, San Francisco, CA). All these antigens were tested on paraffin-embedded sections from cell blocks with a previous step of antigen retrieval. For p27Kip1 assessment, sections were treated twice in a microwave oven for 5 minutes in citrate buffer (pH 6); for Ki-67, sections were first treated with trypsin (Sigma Chemical Co., St. Louis, MO) (0.33 mg/ml) for 1 minute and then twice for 5 minutes in citrate buffer (pH 6) in a microwave oven at 650 W; for cellular cyclin D1, Bouin-fixed sections were treated with trypsin (Sigma Chemical Co.) (0.2 mg/ml) for 5 minutes whereas formalin-fixed sections were treated for 30 minutes in citrate buffer (pH 7) in a microwave oven at 250 W.
Immunocytochemical staining for p27Kip1and Ki-67 was performed by using the ABC method25 (ABC-Elite kit, Vector, Burlingame, California), whereas immunocytochemical staining for cellular cyclin D1 was performed on an automated immunostainer (Ventana Medical Systems, Inc, Tucson, AZ) according to a modified version of the company’s protocols. Positive controls for p27Kip1, Ki-67 and cellular cyclin D1 were used to confirm the adequacy of the staining.
For comparative purposes cyclin D3 was tested on cytospin preparations from all PEL cell lines. Cyclin D3 was detected with the mAb DCS-22 (NeoMarkers, Inc., Fremont, California) and the ABC method.25
HHV-8 v-cyclin was assessed in cytospin preparations using sheep polyclonal v-cyclin-specific antibodies (Bionostics Inc., Toronto, Canada). Cytospins were fixed in acetone-chloroform (1:1) solution for 5 minutes and stored at -80°C until use. Slides were then brought to room temperature; fixed in acetone for 5 minutes at room temperature; air dried; fixed in buffered 10% formalin for 10 minutes at room temperature; rinsed in PBS, pH 7.4; fixed in cold methanol at -20°C for 10 minutes; and then incubated overnight at 4°C with sheep anti-HHV-8 cyclin. After washing, cytospins were incubated with rabbit anti-sheep IgG (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA) and then immunostained by using the ABC method25 (ABC-Elite kit, Vector).
The percentage of cells showing positive nuclear staining for the different antigens was assessed in each case.
Western Blot Analysis
Cells were washed twice in ice-cold phosphate-buffered saline (PBS, pH 7.4), and lysed on ice for 30 minutes in a buffer containing 10 mmol/L Tris-HCl, pH 8.0; 1% Triton X-100; 150 mmol/L NaCl; 1.0 mmol/L EDTA; 1.0 mmol/L phenylmethylsulfonyl fluoride; and 10% glycerol. After centrifugation for 10 minutes at 13,000 rpm, the supernatant was collected and samples were diluted in Laemmli sample buffer containing final concentrations of 125 mmol/L Tris-HCl (pH 6.8), 2% sodium dodecyl sulfate, 10% glycerol, 5% 2-mercaptoethanol, and 0.001% bromphenol blue. Furthermore, total cell lysates were also prepared by direct lysis of cell pellets with Laemmli sample buffer. After boiling for 5 minutes, total cell lysates and/or protein extracts were subjected to 12% sodium dodecyl sulfate-polyacrylamide gel electrophoresis under reducing conditions and transferred to nitrocellulose filters (Sartorius, Göttingen, Germany) which were then blocked by incubation with 5% non-fat dried milk dissolved in Tris-buffered saline–Tween (50 mmol/L Tris-HCl, 150 mmol/L NaCl, pH 7.5, 0.1% Tween-20) for 2 hours under shaking. Membranes were then incubated overnight at room temperature with p27Kip1 or cellular cyclin D1 antibodies or at 4°C with v-cyclin antibodies. After washing in Tris-buffered saline–Tween, filters were incubated with the appropriate secondary antibody, ie, peroxidase-conjugated goat anti-mouse immunoglobulin (Dako EnVision; Dako Corporation, Carpinteria, CA) or peroxidase-conjugated rabbit anti-sheep IgG (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA) for 1 hour at room temperature and then developed using the enhanced chemiluminescence system (ECL; Amersham Pharmacia Biotech), following the manufacturer’s instructions.
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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A total of 18 cases of PEL were immunostained for
p27Kip1 and Ki-67. The results are summarized in
Table 1
. Eighteen out of 18 cases (100%)
showed expression of p27Kip1 (Table 1
, Figure 1
). The cases consistently showed nuclear
p27Kip1 staining of moderate-to-strong intensity
in a large number of tumor cells (median, 55%; range, 30% to 90%).
p27Kip1 expression in PELs occurred regardless of
the generally high proliferative index of the neoplastic population, as
assessed with the proliferation marker Ki-67 (median, 90%; range, 60%
to 100%) (Table 1
, Figure 1
).
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All 18 cases of PEL were immunostained for cellular cyclin D1, whereas immunostaining for HHV-8 v-cyclin was performed in 14 PEL samples for which cytospin preparations were available.
Cellular cyclin D1 scored consistently negative in all PEL samples
investigated. In contrast, cyclin D3 scored positive in all PEL cell
lines. Nuclear staining for cyclin D3 was observed in a large number of
tumor cells (median, 70%; range, 20% to 90%). The intensity of
staining was moderate to strong among the cells. HHV-8 v-cyclin was
found to be expressed in 10 out of 14 samples of PEL (five clinical
samples and five cell lines) (Figure 2)
.
Nuclear staining for HHV-8 v-cyclin was detected in a large number of
tumor cells (median, 80%; range, 60% to 90%); the intensity of the
staining was moderate to weak among the cells.
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Western blot analysis of p27Kip1, cellular
cyclin D1, and HHV-8 v-cyclin was performed in the PEL cell lines
(Table 1)
. All PEL cell lines investigated by this technique scored
positive for the presence of p27Kip1 (Table 1
and
Figure 3
). Conversely, cellular cyclin D1
was not detected in any of the samples tested (Table 1)
. Nine out of
nine PEL cell lines expressed HHV-8 v-cyclin (Table 1
and see Figure 3
for representative results). The signal intensity of HHV-8 v-cyclin was
variable among different PEL cell lines, and was higher in BC-1, BC-2,
BC-3, BCP-1, and BCBL-1, whereas was weaker in the remaining four cell
lines.
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A total of ten cases of HHV-8-negative secondary lymphomatous
effusions were immunostained for p27Kip1, Ki-67,
and cellular cyclin D1. The results are summarized in Table 1
. Overall,
secondary lymphomatous effusions displayed an inverse correlation
between the percentage of tumor cells expressing
p27Kip1 and that of tumor cells expressing the
proliferation marker Ki-67 (Table 1)
. In all cases, reactive small
lymphocytes admixed with the tumor cells exhibited strong nuclear
positivity for p27Kip1. Cellular cyclin D1
expression was completely negative in all 10 cases tested (Table 1)
.
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Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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Our results unequivocally define that PEL is characterized by the co-existence of p27Kip1 overexpression and high proliferation index, as detected by the Ki-67 nuclear antigen. The consistent association between p27Kip1 overexpression and high proliferation index may be considered a peculiarity of PEL and is otherwise exceptional in other lymphoid tissues. In fact, consistent with the role of p27Kip1 as a negative regulator of cell cycle progression, reactive lymphoid tissues and most tissue-based B-cell NHL analyzed to date, with the exception of a small subset of B-DLCL and BL cases,13,27 display an inverse relation between p27Kip1 expression and growth fraction measured by Ki-67 staining.13-15 Co-expression of p27Kip1 and Ki-67 is a selective feature of PEL also when considering lymphomas involving the serous body cavities, because HHV-8-negative secondary lymphomatous effusions generally show very weak p27Kip1 expression and high proliferative rate.
The precise mechanism for the co-existence of p27Kip1 expression and high proliferation index in PEL is not formally clarified. However, a potential explanation may lie in differences in the biochemical properties of HHV-8 v-cyclin as opposed to cellular D-type cyclins. In fact, the interaction between HHV-8 v-cyclin and p27Kip1 in PEL seems to differ in some respects from that observed between cellular D-type cyclins and p27Kip1 in other B-cell lymphomas.15,27 Experimental studies indicate that the HHV-8 v-cyclin forms complexes with CDK28,29 which are able to exert functional activity on downstream targets also shared by CDK/cyclin D complexes.28,30 Unlike CDK/cyclin D complexes, however, CDK/v-cyclin activity is resistant to inhibition by CDK inhibitors, including p27Kip1.31 Overall, these observations suggest a model in which PEL cells express high levels of p27Kip1which, however, is unable to inactivate HHV-8 v-cyclin and, therefore, is unable to exert its physiological function of negative regulator of cell cycle progression.
The model of p27Kip1/cyclin interactions proposed for PEL differs significantly from that of other B-cell NHL in which cyclin D plays a major pathogenetic role.15,27 In mantle cell lymphoma, the t(11;14) translocation leads to overexpression of cyclin D1, which in turn sequesters p27Kip1, thus causing its functional inactivation.15,32 Conversely, PEL escape from p27Kip1 mediated control through substitution of the p27Kip1 physiological target cyclin D with the HHV-8 encoded v-cyclin that is resistant to p27Kip1 activity.31 The differences in p27Kip1/cyclin interactions may also explain the different expression pattern of p27Kip1 in PEL as opposed to mantle cell lymphoma. In fact, the p27Kip1 protein is immunologically undetectable when bound to cyclin D1,15,32 thus explaining the abrogation of its expression in mantle cell lymphoma but not in PEL.
Several issues remain to be clarified with respect to the interactions between p27Kip1 and HHV-8 v-cyclin. For example, in PEL cell lines, the CDK/v-cyclin complexes phosphorylate p27Kip1 on a C-terminal threonine that is implicated in destabilization of this CDK inhibitor.33 Because our results show that p27Kip1 is expressed at high levels in PEL cells in vivo, future studies need to address the detailed balance between p27Kip1 production and degradation in HHV-8-positive lymphomas, resulting in p27Kip1 overexpression despite destabilization of the molecule.
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Footnotes |
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Supported in part by ISS, II Programma nazionale di ricerca sull’AIDS —Progetto Patologia clinica e terapia dell’AIDS, Rome, Italy (to A. C. and G. G.). P. J. B. was supported in part by the Public Health Service grant R01CA75535 from the National Institutes of Health, Department of Health and Human Services. D. B. was supported by a fellowship from Associazione Italiana per la Ricerca sul Cancro (AIRC), Milan, Italy.
Accepted for publication December 9, 1999.
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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