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Carcinogenesis, Vol. 22, No. 10, 1583-1591, October 2001
© 2001 Oxford University Press


COMMENTARY

Role of the high mobility group A* proteins in human lipomas

Monica Fedele1, Sabrina Battista1, Guidalberto Manfioletti2, Carlo Maria Croce3, Vincenzo Giancotti2 and Alfredo Fusco1,4,5

1 Centro di Endocrinologia ed Oncologia Sperimentale del Consiglio Nazionale delle Ricerche c/o Dipartimento di Biologia e Patologia Cellulare e Molecolare, Facoltà di Medicina e Chirurgia, Università degli Studi di Napoli, Via Pansini, 5, I-80131 Naples, Italy, Istituto Nazionale dei Tumori Fondazione Senatore Pascale, via M. Semmola, I-80131 Naples, Italy,
2 Dipartimento di Biochimica, Biofisica e Chimica delle Macromolecole, University of Trieste, Italy,
3 Kimmel Cancer Center, Jefferson Medical College, Philadelphia, PE 19107, USA and
4 Dipartimento di Medicina Sperimentale e Clinica, Facoltà di Medicina e Chirurgia di Catanzaro, Università degli Studi di Catanzaro, via Tommaso Campanella 5, I-88100 Catanzaro, Italy

The HMGA family is comprised of four proteins: HMGA1a, HMGA1b, HMGA1c and HMGA2. The first three proteins are products of the same gene, HMGA1, generated through an alternative splicing mechanism. The HMGA proteins are involved in the regulation of chromatin structure and HMGA DNA-binding sites have been identified in functional regions of many gene promoters. Rearrangements of the HMGA2 gene have been frequently detected in human benign tumors of mesenchymal origin including lipomas. 12q13-15 chromosomal translocations involving the HMGA2 gene locus, account for these rearrangements. The HMGA proteins have three AT-hook domains and an acidic C-terminal tail. The HMGA2 modifications consist in the loss of the C-terminal tail and fusion with ectopic sequences. A pivotal role of the HMGA2 rearrangements in the process of lipomagenesis is suggested by experiments showing that transgenic mice carrying a truncated HMGA2 gene showed a giant phenotype together with abdominal/pelvic lipomatosis. As HMGA2 null mice showed a great reduction in fat tissue, a positive role of the HMGA2 gene in adipocytic cell proliferation is proposed. More recently, similar alterations of the HMGA1 gene have been described. As the block of the HMGA1 protein synthesis induces an increase in growth rate of the pre-adipocytic cell line 3T3-L1, we suggest a negative role of the HMGA1 proteins in adipocytic cell growth and, therefore, we propose that adipocytic cell growth derives from the balance of the HMGA1 and HMGA2 protein functions.


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