Santonocito C, Capizzi R, Concolino P, Lavieri M M, Paradisi A, Gentileschi S, Torti E, Rutella S, Rocchetti S, Di Carlo A, Di Stasio E, Ameglio F, Zuppi C, Capoluongo E
Laboratory of Molecular Biology, Institute of Biochemistry and Clinical Biochemistry, Catholic University, Largo A Gemeli 8, 00168 Rome, Italy.
Br J Dermatol. 2007 Feb;156(2):277-82. doi: 10.1111/j.1365-2133.2006.07620.x.
Literature data report an association between some vitamin D receptor (VDR) polymorphisms and different kinds of tumours, including malignant melanoma (MM). Only three VDR polymorphisms (FokI, TaqI and A-1012G) have been investigated in association with the presence of cutaneous MM or the development of metastases.
The present paper analyses for the first time the association between BsmI polymorphism and MM prevalence together with Breslow thickness. In addition, the FokI single nucleotide polymorphism was also determined.
One hundred and one patients with MM and 101 healthy donors matched for age and sex were enrolled. Molecular VDR typing was performed by means of restriction fragment length polymorphism analysis.
All cases and controls were in Hardy-Weinberg equilibrium for BsmI, FokI and A-1012G. Significant associations were found between the BsmI bb genotype frequency and MM (P = 0.02) along with Breslow thickness (P = 0.001). This same behaviour was not observed for the FokI or A-1012G polymorphisms. Multivariate logistic regression analysis confirmed these significant results after correction for age, gender, skin type and MM localization.
Although the biological meaning of the effects exerted by BsmI polymorphism is still under debate, the statistical association found in the present study suggests that further work should be done to verify this variant as a possible risk marker for MM and its aggressiveness, also considering that the real association may be due to other unknown genes linked to the BsmI b allele.
文献数据报道了某些维生素D受体(VDR)多态性与包括恶性黑色素瘤(MM)在内的不同类型肿瘤之间的关联。仅对三种VDR多态性(FokI、TaqI和A - 1012G)与皮肤MM的存在或转移的发生之间的关联进行了研究。
本文首次分析了BsmI多态性与MM患病率以及Breslow厚度之间的关联。此外,还测定了FokI单核苷酸多态性。
招募了101例MM患者和101名年龄和性别相匹配的健康供体。通过限制性片段长度多态性分析进行VDR分子分型。
所有病例和对照在BsmI、FokI和A - 1012G方面均处于Hardy - Weinberg平衡。发现BsmI bb基因型频率与MM(P = 0.02)以及Breslow厚度(P = 0.001)之间存在显著关联。FokI或A - 1012G多态性未观察到相同的情况。在对年龄、性别、皮肤类型和MM定位进行校正后,多变量逻辑回归分析证实了这些显著结果。
尽管BsmI多态性所产生影响的生物学意义仍在争论中,但本研究中发现的统计学关联表明,应进一步开展工作以验证该变异作为MM及其侵袭性的可能风险标志物,同时考虑到真正的关联可能归因于与BsmI b等位基因连锁的其他未知基因。