TY - JOUR
T1 - Melanotransferrin
T2 - Search for a function
AU - Rahmanto, Yohan Suryo
AU - Bal, Sumeet
AU - Loh, Kim H.
AU - Yu, Yu
AU - Richardson, Des R.
N1 - Funding Information:
YSR and DRR were supported by a Cancer Institute New South Wales Early Career Development Fellowship [ 08/ECF/1-36 ] and National Health and Medical Research Council of Australia Senior Principal Research Fellowship [ 570829 ], respectively. This work was supported by a National Health and Medical Research Council of Australia Project Grant [ 570951 ] to DRR and YSR. We would like to kindly acknowledge Dr. Danuta Kalinowksi from the Iron Metabolism and Chelation Program, Department of Pathology for her kind help in reviewing the manuscript prior to submission.
PY - 2012/3
Y1 - 2012/3
N2 - Background Melanotransferrin was discovered in the 1980s as one of the first melanoma tumour antigens. The molecule is a transferrin homologue that is found predominantly bound to the cell membrane by a glycosyl- phosphatidylinositol anchor. MTf was described as an oncofoetal antigen expressed in only small quantities in normal tissues, but in much larger amounts in neoplastic cells. Several diseases are associated with expression of melanotransferrin, including melanoma and Alzheimer's disease, although the significance of the protein to the pathogenesis of these conditions remains unclear. Scope of review In this review, we discuss the roles of melanotransferrin in physiological and pathological processes and its potential use as an immunotherapy. Major conclusions Although the exact biological functions of melanotransferrin remain elusive, a growing number of roles have been attributed to the protein, including iron transport/metabolism, angiogenesis, proliferation, cellular migration and tumourigenesis. General significance The high expression of melanotransferrin in several disease states, particularly malignant melanoma, remains intriguing and may have clinical significance. Further studies on the biology of this protein may provide new insights as well as potential therapeutic avenues for cancer treatment. This article is part of a Special Issue entitled Transferrins: Molecular mechanisms of iron transport and disorders.
AB - Background Melanotransferrin was discovered in the 1980s as one of the first melanoma tumour antigens. The molecule is a transferrin homologue that is found predominantly bound to the cell membrane by a glycosyl- phosphatidylinositol anchor. MTf was described as an oncofoetal antigen expressed in only small quantities in normal tissues, but in much larger amounts in neoplastic cells. Several diseases are associated with expression of melanotransferrin, including melanoma and Alzheimer's disease, although the significance of the protein to the pathogenesis of these conditions remains unclear. Scope of review In this review, we discuss the roles of melanotransferrin in physiological and pathological processes and its potential use as an immunotherapy. Major conclusions Although the exact biological functions of melanotransferrin remain elusive, a growing number of roles have been attributed to the protein, including iron transport/metabolism, angiogenesis, proliferation, cellular migration and tumourigenesis. General significance The high expression of melanotransferrin in several disease states, particularly malignant melanoma, remains intriguing and may have clinical significance. Further studies on the biology of this protein may provide new insights as well as potential therapeutic avenues for cancer treatment. This article is part of a Special Issue entitled Transferrins: Molecular mechanisms of iron transport and disorders.
KW - Cell proliferation
KW - Iron
KW - Keywords
KW - Melanotransferrin
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U2 - 10.1016/j.bbagen.2011.09.003
DO - 10.1016/j.bbagen.2011.09.003
M3 - Review article
C2 - 21933697
AN - SCOPUS:84857363706
SN - 0304-4165
VL - 1820
SP - 237
EP - 243
JO - Biochimica et Biophysica Acta - General Subjects
JF - Biochimica et Biophysica Acta - General Subjects
IS - 3
ER -