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Published in: Cancer Immunology, Immunotherapy 9/2012

01-09-2012 | Original article

Evaluation of CTLA-4 expression and relevance as a novel prognostic factor in patients with non-small cell lung cancer

Authors: Sandra Salvi, Vincenzo Fontana, Simona Boccardo, Domenico Franco Merlo, Edoardo Margallo, Stefania Laurent, Anna Morabito, Erika Rijavec, Maria Giovanna Dal Bello, Marco Mora, Giovanni Battista Ratto, Francesco Grossi, Mauro Truini, Maria Pia Pistillo

Published in: Cancer Immunology, Immunotherapy | Issue 9/2012

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Abstract

The role of CTLA-4 in negative regulation of T-cell mediated immune response is particularly well established. Much less is known about its expression and function in tumour cells, and to our knowledge, no data are available on its possible impact on prognosis of NSCLC patients. We investigated CTLA-4 expression and prognostic role in 81 patients with radically resected stage I–III NSCLC. The analysis was performed by tissue microarray immunohistochemistry, and the median H-score of 20 was used as a threshold to define CTLA-4 overexpressing tumours. Correlation with standard prognostic factors was performed by using absolute and relative fold change indexes. Hazard ratios (HR) and corresponding 95% confidence limits (95% CL) were computed through the Cox model. A higher frequency of CTLA-4 overexpression (>20) was found in non-squamous than in squamous NSCLC (52.8 vs. 35.7%) and in Ki67 ≤ 15 expressing tumours, as compared to those with Ki67 > 15 (51.5 vs. 38.7%). A reduced death rate was found in CTLA-4 overexpressing tumours (HR = 0.60, 95% CL = 0.28/1.23), and a further decrease was observed when considering tumours with CTLA-4 > 20 and Ki67 ≤ 15, in comparison with tumours with CTLA-4 ≤ 20 and Ki67 > 15 (HR = 0.41; 95% CL = 0.15/1.13). Our observational and exploratory study provides a first and promising indication for an independent prognostic effect of CTLA-4 overexpression in radically resected NSCLC. We presume that this effect relies on modulation of the interaction of microscopic disease with CTLA-4-ligands expressing cells leading to NSCLC cell death.
Literature
1.
go back to reference Krummel MF, Allison JP (1996) CTLA-4 engagement inhibits IL-2 accumulation and cell cycle progression upon activation of resting T cells. J Exp Med 183:2533–2540PubMedCrossRef Krummel MF, Allison JP (1996) CTLA-4 engagement inhibits IL-2 accumulation and cell cycle progression upon activation of resting T cells. J Exp Med 183:2533–2540PubMedCrossRef
2.
go back to reference Brunner MC, Chambers CA, Chan FK, Hanke J, Winoto A, Allison JP (1999) CTLA-4-Mediated inhibition of early events of T cell proliferation. J Immunol 162:5813–5820PubMed Brunner MC, Chambers CA, Chan FK, Hanke J, Winoto A, Allison JP (1999) CTLA-4-Mediated inhibition of early events of T cell proliferation. J Immunol 162:5813–5820PubMed
3.
go back to reference Teft WA, Kirchhof MG, Madrenas J (2006) A molecular perspective of CTLA-4 function. Annu Rev Immunol 24:65–97PubMedCrossRef Teft WA, Kirchhof MG, Madrenas J (2006) A molecular perspective of CTLA-4 function. Annu Rev Immunol 24:65–97PubMedCrossRef
4.
go back to reference Carreno BM, Bennett F, Chau TA, Ling V, Luxenberg D, Jussif J et al (2000) CTLA-4 (CD152) can inhibit T cell activation by two different mechanisms depending on its level of cell surface expression. J Immunol 165:1352–1356PubMed Carreno BM, Bennett F, Chau TA, Ling V, Luxenberg D, Jussif J et al (2000) CTLA-4 (CD152) can inhibit T cell activation by two different mechanisms depending on its level of cell surface expression. J Immunol 165:1352–1356PubMed
5.
go back to reference Jain N, Nguyen H, Chambers C, Kang J (2010) Dual function of CTLA-4 in regulatory T cells and conventional T cells to prevent multiorgan autoimmunity. Proc Natl Acad Sci USA 107:1524–1528PubMedCrossRef Jain N, Nguyen H, Chambers C, Kang J (2010) Dual function of CTLA-4 in regulatory T cells and conventional T cells to prevent multiorgan autoimmunity. Proc Natl Acad Sci USA 107:1524–1528PubMedCrossRef
6.
go back to reference Merlo A, Tenca C, Fais F, Battini L, Ciccone E, Grossi CE, Saverino D (2005) Inhibitory receptors CD85j, LAIR-1, and CD152 down-regulate immunoglobulin and cytokine production by human B lymphocytes. Clin Diagn Lab Immunol 12:705–712PubMed Merlo A, Tenca C, Fais F, Battini L, Ciccone E, Grossi CE, Saverino D (2005) Inhibitory receptors CD85j, LAIR-1, and CD152 down-regulate immunoglobulin and cytokine production by human B lymphocytes. Clin Diagn Lab Immunol 12:705–712PubMed
7.
go back to reference Wang XB, Giscombe R, Yan Z, Heiden T, Xu D, Lefvert AK (2002) Expression of CTLA-4 by human monocytes. Scand J Immunol 55:53–60PubMedCrossRef Wang XB, Giscombe R, Yan Z, Heiden T, Xu D, Lefvert AK (2002) Expression of CTLA-4 by human monocytes. Scand J Immunol 55:53–60PubMedCrossRef
8.
go back to reference Laurent S, Carrega P, Saverino D, Piccioli P, Camoriano M, Morabito A et al (2010) CTLA-4 is expressed by human monocyte-derived dendritic cells and regulates their functions. Hum Immunol 71:934–941PubMedCrossRef Laurent S, Carrega P, Saverino D, Piccioli P, Camoriano M, Morabito A et al (2010) CTLA-4 is expressed by human monocyte-derived dendritic cells and regulates their functions. Hum Immunol 71:934–941PubMedCrossRef
9.
go back to reference Kaufman KA, Bowen JA, Tsai AF, Bluestone JA, Hunt JS, Ober C (1999) The CTLA-4 gene is expressed in placental fibroblasts. Mol Hum Reprod 5:84–87PubMedCrossRef Kaufman KA, Bowen JA, Tsai AF, Bluestone JA, Hunt JS, Ober C (1999) The CTLA-4 gene is expressed in placental fibroblasts. Mol Hum Reprod 5:84–87PubMedCrossRef
10.
go back to reference Nagaraju K, Raben N, Villalba ML, Danning C, Loeffler LA, Lee E et al (1999) Costimulatory markers in muscle of patients with idiopathic inflammatory myopathies and in cultured muscle cells. Clin Immunol 92:161–169PubMedCrossRef Nagaraju K, Raben N, Villalba ML, Danning C, Loeffler LA, Lee E et al (1999) Costimulatory markers in muscle of patients with idiopathic inflammatory myopathies and in cultured muscle cells. Clin Immunol 92:161–169PubMedCrossRef
11.
go back to reference Pistillo MP, Tazzari PL, Palmisano GL, Pierri I, Bolognesi A, Ferlito F et al (2003) CTLA-4 is not restricted to the lymphoid cell lineage and can function as a target molecule for apoptosis induction of leukemic cells. Blood 101:202–209PubMedCrossRef Pistillo MP, Tazzari PL, Palmisano GL, Pierri I, Bolognesi A, Ferlito F et al (2003) CTLA-4 is not restricted to the lymphoid cell lineage and can function as a target molecule for apoptosis induction of leukemic cells. Blood 101:202–209PubMedCrossRef
12.
go back to reference Joshi AD, Hegde GV, Dickinson JD, Mittal AK, Lynch JC, Eudy JD et al (2007) ATM, CTLA4, MNDA, and HEM1 in high versus low CD38 expressing B-cell chronic lymphocytic leukemia. Clin Cancer Res 13:5295–5304PubMedCrossRef Joshi AD, Hegde GV, Dickinson JD, Mittal AK, Lynch JC, Eudy JD et al (2007) ATM, CTLA4, MNDA, and HEM1 in high versus low CD38 expressing B-cell chronic lymphocytic leukemia. Clin Cancer Res 13:5295–5304PubMedCrossRef
13.
go back to reference Kosmaczewska A, Ciszak L, Suwalska K, Wolowiec D, Frydecka I (2005) CTLA-4 overexpression in CD19+/CD5+ cells correlates with the level of cell cycle regulators and disease progression in B-CLL patients. Leukemia 19:301–314PubMedCrossRef Kosmaczewska A, Ciszak L, Suwalska K, Wolowiec D, Frydecka I (2005) CTLA-4 overexpression in CD19+/CD5+ cells correlates with the level of cell cycle regulators and disease progression in B-CLL patients. Leukemia 19:301–314PubMedCrossRef
14.
go back to reference Mao H, Zhang L, Yang Y, Zuo W, Bi Y, Gao W et al (2010) New insights of CTLA-4 into its biological function in breast cancer. Curr Cancer Drug Targets 10:728–736PubMedCrossRef Mao H, Zhang L, Yang Y, Zuo W, Bi Y, Gao W et al (2010) New insights of CTLA-4 into its biological function in breast cancer. Curr Cancer Drug Targets 10:728–736PubMedCrossRef
15.
go back to reference Contardi E, Palmisano GL, Tazzari PL, Martelli AM, Falà F, Fabbi M et al (2005) CTLA-4 is constitutively expressed on tumour cells and can trigger apoptosis upon ligand interaction. Int J Cancer 117:538–550PubMedCrossRef Contardi E, Palmisano GL, Tazzari PL, Martelli AM, Falà F, Fabbi M et al (2005) CTLA-4 is constitutively expressed on tumour cells and can trigger apoptosis upon ligand interaction. Int J Cancer 117:538–550PubMedCrossRef
16.
go back to reference Shah KV, Chien AJ, Yee C, Moon RT (2008) CTLA-4 is a direct target of Wnt/beta-catenin signaling and is expressed in human melanoma tumours. J Invest Dermatol 128:2870–2879PubMedCrossRef Shah KV, Chien AJ, Yee C, Moon RT (2008) CTLA-4 is a direct target of Wnt/beta-catenin signaling and is expressed in human melanoma tumours. J Invest Dermatol 128:2870–2879PubMedCrossRef
17.
go back to reference Hodi FS, O’Day SJ, McDermott DF, Weber RW, Sosman JA, Haanen JB et al (2010) Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med 19(363):711–723CrossRef Hodi FS, O’Day SJ, McDermott DF, Weber RW, Sosman JA, Haanen JB et al (2010) Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med 19(363):711–723CrossRef
18.
go back to reference Tarhini A, Lo E, Minor DR (2010) Releasing the brake on the immune system: ipilimumab in melanoma and other tumours. Cancer Biother Radiopharm 25:601–613PubMedCrossRef Tarhini A, Lo E, Minor DR (2010) Releasing the brake on the immune system: ipilimumab in melanoma and other tumours. Cancer Biother Radiopharm 25:601–613PubMedCrossRef
19.
go back to reference Leach DR, Krummel MF, Allison JP (1996) Enhancement of antitumour immunity by CTLA-4 blockade. Science 27:1734–1736CrossRef Leach DR, Krummel MF, Allison JP (1996) Enhancement of antitumour immunity by CTLA-4 blockade. Science 27:1734–1736CrossRef
20.
go back to reference Maker AV, Phan GQ, Attia P, Yang JC, Sherry RM, Topalian SL et al (2005) Tumour regression and autoimmunity in patients treated with cytotoxic T lymphocyte-associated antigen 4 blockade and interleukin 2: a phase I/II study. Ann Surg Oncol 12:1005–1016PubMedCrossRef Maker AV, Phan GQ, Attia P, Yang JC, Sherry RM, Topalian SL et al (2005) Tumour regression and autoimmunity in patients treated with cytotoxic T lymphocyte-associated antigen 4 blockade and interleukin 2: a phase I/II study. Ann Surg Oncol 12:1005–1016PubMedCrossRef
21.
go back to reference Page DB, Yuan J, Wolchok JD (2010) Targeting cytotoxic T-lymphocyte antigen 4 in immunotherapies for melanoma and other cancers. Immunotherapy 2(3):367–379PubMedCrossRef Page DB, Yuan J, Wolchok JD (2010) Targeting cytotoxic T-lymphocyte antigen 4 in immunotherapies for melanoma and other cancers. Immunotherapy 2(3):367–379PubMedCrossRef
22.
go back to reference Zheng H, Li Y, Wang X, Zhang X, Wang X (2010) Expression and significance of gp96 and immune-related gene CTLA-4, CD8 in lung cancer tissues. Zhongguo Fei Ai Za Zhi 13:790–794PubMed Zheng H, Li Y, Wang X, Zhang X, Wang X (2010) Expression and significance of gp96 and immune-related gene CTLA-4, CD8 in lung cancer tissues. Zhongguo Fei Ai Za Zhi 13:790–794PubMed
23.
go back to reference Naruke T, Suemasu K, Ishikawa S (1978) Lymph node mapping and curability at various levels of metastasis in resected lung cancer. J Thorac Cardiovasc Surg 76:832–839PubMed Naruke T, Suemasu K, Ishikawa S (1978) Lymph node mapping and curability at various levels of metastasis in resected lung cancer. J Thorac Cardiovasc Surg 76:832–839PubMed
24.
go back to reference Sobin LH, Wittekind CH (eds) (1997) TNM classification of malignant tumours, 5th edn. Wiley-Liss, New York, pp 59–62 Sobin LH, Wittekind CH (eds) (1997) TNM classification of malignant tumours, 5th edn. Wiley-Liss, New York, pp 59–62
25.
go back to reference Sobin LH and Pathologists from 14 Countries World Health Organization International Histological Classification of Tumours (1999) Histological typing of lung and pleural tumours, 3rd edn. Springer, Geneva Sobin LH and Pathologists from 14 Countries World Health Organization International Histological Classification of Tumours (1999) Histological typing of lung and pleural tumours, 3rd edn. Springer, Geneva
26.
go back to reference Tokuhara T, Hattori N, Ishida H, Hirai T, Higashiyama M, Kodama K, Miyake M (2006) Clinical significance of aminopeptidase N in non-small cell lung cancer. Clin Cancer Res 1(12):3971–3978CrossRef Tokuhara T, Hattori N, Ishida H, Hirai T, Higashiyama M, Kodama K, Miyake M (2006) Clinical significance of aminopeptidase N in non-small cell lung cancer. Clin Cancer Res 1(12):3971–3978CrossRef
27.
go back to reference Dertsiz L, Ozbilim G, Kayisli Y, Gokhan GA, Demircan A, Kayisli UA (2005) Differential expression of VASP in normal lung tissue and lung adenocarcinomas. Thorax 60:576–581PubMedCrossRef Dertsiz L, Ozbilim G, Kayisli Y, Gokhan GA, Demircan A, Kayisli UA (2005) Differential expression of VASP in normal lung tissue and lung adenocarcinomas. Thorax 60:576–581PubMedCrossRef
28.
go back to reference Hosmer D, Lemeshow S (1999) Applied survival analysis: regression modeling of time to event data. Wiley, New York Hosmer D, Lemeshow S (1999) Applied survival analysis: regression modeling of time to event data. Wiley, New York
29.
30.
go back to reference Bienz M (2005) Beta-catenin: a pivot between cell adhesion and Wnt signalling. Curr Biol 15:R64–R67PubMedCrossRef Bienz M (2005) Beta-catenin: a pivot between cell adhesion and Wnt signalling. Curr Biol 15:R64–R67PubMedCrossRef
31.
go back to reference Gavert N, Ben-Ze’ev A (2007) Beta-catenin signaling in biological control and cancer. J Cell Biochem 102:820–828PubMedCrossRef Gavert N, Ben-Ze’ev A (2007) Beta-catenin signaling in biological control and cancer. J Cell Biochem 102:820–828PubMedCrossRef
32.
go back to reference Liu D, Huang C, Kameyama K, Hayashi E, Yamauchi A, Kobayashi S, Yokomise H (2001) E-cadherin expression associated with differentiation and prognosis in patients with non-small cell lung cancer. Ann Thorac Surg 71:949–955PubMedCrossRef Liu D, Huang C, Kameyama K, Hayashi E, Yamauchi A, Kobayashi S, Yokomise H (2001) E-cadherin expression associated with differentiation and prognosis in patients with non-small cell lung cancer. Ann Thorac Surg 71:949–955PubMedCrossRef
33.
go back to reference Kase S, Sugio K, Yamazaki K, Okamoto T, Yano T, Sugimachi K (2000) Expression of E-cadherin and beta-catenin in human non-small cell lung cancer and the clinical significance. Clin Cancer Res 6:4789–4796PubMed Kase S, Sugio K, Yamazaki K, Okamoto T, Yano T, Sugimachi K (2000) Expression of E-cadherin and beta-catenin in human non-small cell lung cancer and the clinical significance. Clin Cancer Res 6:4789–4796PubMed
34.
go back to reference Gerdes J, Lemke H, Baisch H, Wacker HH, Schwab U, Stein H (1984) Cell cycle analysis of a cell proliferation-associated human nuclear antigen defined by the monoclonal antibody Ki-67. J Immunol 133:1710–1715PubMed Gerdes J, Lemke H, Baisch H, Wacker HH, Schwab U, Stein H (1984) Cell cycle analysis of a cell proliferation-associated human nuclear antigen defined by the monoclonal antibody Ki-67. J Immunol 133:1710–1715PubMed
35.
go back to reference Martin B, Paesmans M, Mascaux C, Berghmans T, Lothaire P, Meert AP et al (2004) Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis. Br J Cancer 91:2018–2025PubMedCrossRef Martin B, Paesmans M, Mascaux C, Berghmans T, Lothaire P, Meert AP et al (2004) Ki-67 expression and patients survival in lung cancer: systematic review of the literature with meta-analysis. Br J Cancer 91:2018–2025PubMedCrossRef
36.
go back to reference Zou W, Chen L (2005) Inhibitory B7-family molecules in the tumour microenvironment. Nat Rev Immunol 8:467–477CrossRef Zou W, Chen L (2005) Inhibitory B7-family molecules in the tumour microenvironment. Nat Rev Immunol 8:467–477CrossRef
37.
Metadata
Title
Evaluation of CTLA-4 expression and relevance as a novel prognostic factor in patients with non-small cell lung cancer
Authors
Sandra Salvi
Vincenzo Fontana
Simona Boccardo
Domenico Franco Merlo
Edoardo Margallo
Stefania Laurent
Anna Morabito
Erika Rijavec
Maria Giovanna Dal Bello
Marco Mora
Giovanni Battista Ratto
Francesco Grossi
Mauro Truini
Maria Pia Pistillo
Publication date
01-09-2012
Publisher
Springer-Verlag
Published in
Cancer Immunology, Immunotherapy / Issue 9/2012
Print ISSN: 0340-7004
Electronic ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-012-1211-y

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