Increased Insulin-Like Growth Factor 1 Receptor Protein Expression and Gene Copy Number in Small Cell Lung Cancer

• Published in: Journal of thoracic oncology Vol. 5; no. 12; pp. 1905 - 1911
• Main Authors: Badzio, Andrzej, Wynes, Murry W., Dziadziuszko, Rafal, Merrick, Daniel T., Pardo, Marta, Rzyman, Witold, Kowalczyk, Anna, Singh, Shalini, Ranger-Moore, James, Manriquez, Guadalupe, Gaire, Fabien, Jassem, Jacek, Hirsch, Fred R.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2010; International Association for the Study of Lung Cancer
• Subjects: Adult; Aged; Aged, 80 and over; Female; Gene copy number; Gene Dosage; Humans; IGF1R; Lung cancer; Lung Neoplasms - chemistry; Lung Neoplasms - genetics; Lung Neoplasms - therapy; Male; Middle Aged; Prognosis; Protein expression; Receptor, IGF Type 1 - analysis; Receptor, IGF Type 1 - antagonists & inhibitors; Receptor, IGF Type 1 - genetics; Receptor, IGF Type 1 - physiology; Signal Transduction; Small Cell Lung Carcinoma - chemistry; Small Cell Lung Carcinoma - genetics; Small Cell Lung Carcinoma - therapy; Protein expression; Gene copy number; Prognosis; Lung cancer; IGF1R
• ISSN: 1556-0864; 1556-1380
• DOI: 10.1097/JTO.0b013e3181f38f57

Identification of new therapies in small cell lung cancer (SCLC) is urgently needed. Insulin-like growth factor 1 receptor (IGF1R) is a tyrosine kinase receptor implicated in the pathogenesis of several malignancies and is potentially an attractive target for anticancer treatment. Knowledge about IGF1R protein expression, gene copy number, and the prognostic relevance of these features in SCLC is limited. We analyzed IGF1R protein expression and gene copy number in primary tumors from 90 patients with SCLC (67 men and 23 women) who underwent pulmonary resection. IGF1R expression assessed by immunohistochemistry with H scores from 0 to 400 was evaluable in 84 patients and IGF1R gene copy number assessed by silver in situ hybridization technique in 81 patients. Median H score for IGF1R protein expression was 88 (range, 0–400), and the proportion of positive immunostaining using cutoff H score of 10 was 74%. Increased IGF1R gene copy number (an average of four or more copies per cell) was found in 15 cases (18.5%), five of whom (6.2%) showed gene amplification. There was a significant correlation between protein expression and gene copy number (r = 0.49, p < 0.005). IGF1R expression and gene copy number did not associate with clinicopathological factors such as patient age, tumor size, lymph node involvement, stage, and survival. SCLC is characterized by frequent high-IGF1R protein expression, increased gene copy number, and occasional occurrence of true gene amplification. These features may have important implications for future anti-IGF1R therapeutic approaches.