## Abstract The pathogenesis of sporadic insulinomas is not clear, and there are no reliable genetic determinants that are useful to distinguish malignant and benign forms of this tumor. It was reported that 1q LOH might contribute to pathogenesis in gastrinomas and was correlated with tumor progre
X-chromosome loss of heterozygosity frequently occurs in gastrinomas and is correlated with aggressive tumor growth
✍ Scribed by Yuan-Jia Chen; Alexander Vortmeyer; Zhengping Zhuang; Fathia Gibril; Robert T. Jensen
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 237 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0008-543X
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✦ Synopsis
Abstract
BACKGROUND
Recent studies have shown that tumor growth, rather than hormone overproduction, is the leading cause of death among patients with gastrinomas and other malignant gastrointestinal endocrine tumors. No patient/laboratory characteristics accurately predict which tumors will exhibit aggressive growth. Furthermore, little is known regarding the molecular pathogenesis of these tumors. X‐chromosome loss of heterozygosity (LOH) occurs in some nonendocrine tumors, and its presence can be associated with aggressive growth/decreased survival. Data on X‐chromosome LOH in gastrointestinal endocrine tumors are conflicting. Therefore, the purpose of the current study was to determine whether X‐chromosome LOH occurred in gastrinomas and, if so, whether it was correlated with tumor growth, tumor behavior, and/or prognosis.
METHODS
X chromosome allelotyping was performed using 12 microsatallite markers spaced throughout the chromosome using DNA from leukocytes and microdissected gastrinoma specimens from 16 female patients. The presence of X‐chromosome LOH was analyzed for correlations with clinical and laboratory tumor characteristics as well as tumor growth characteristics.
RESULTS
Nine gastrinoma specimens (56%) had X‐chromosome LOH, ranging from 6% to 23% at the 12 different loci studied. X‐chromosome LOH was significantly associated with aggressive postoperative tumor growth, increased primary tumor size, and pancreatic primaries. In 6 tumor specimens, LOH occurred on Xp22.1–22.3 over a 28.4‐centimorgan region.
CONCLUSIONS
X‐chromosome LOH was common in gastrinoma specimens from female patients, and its presence was found to be a potentially useful molecular/genetic prognostic factor for aggressive growth. Cancer 2004;100:1379–87. Published 2004 American Cancer Society.
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## Abstract We previously applied arbitrarily primed polymerase chain reaction DNA fingerprinting to identify molecular genetic alterations in primary breast carcinomas. One of the most frequently observed fingerprint alterations was a reduction in the intensity of the MCG1‐B2 band in 32% of tumors