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The degree of chromosomal losses and the presence of microsatellite instability (MSI) in gastric carcinomas have been categorized into low-risk (low-level loss and MSI) and high-risk (baseline-and high-level losses) genotypes. With the aim of making a preoperative diagnosis, this study confirmed the stem line genotype that is common over an entire tumor as well as in a single biopsy specimen. Biopsy specimens were obtained from 91 gastric carcinoma patients and examined for their microsatellite genotypes using a panel of 41 microsatellite markers on 8 cancer-associated chromosomes. The genotype of the biopsy specimens was compared with that of a surgical specimen, which had been multifocally examined for its intratumoral heterogeneity. Of the 91 pairs of biopsy and surgical specimens, 87 (96%) containing either the same (60 cases) or a similar (17 cases) number of chromosomal losses were categorized into the same microsatellite genotype, and the remaining 4 pairs (4%) were classified into a different genotype. The surgical specimens showed that an extraserosal invasion and lymph node metastasis are frequently associated with either a high-level (4 or more) of chromosomal losses irrespective of the tumor size (73% and 85%) or the large carcinomas > 5 cm in diameter irrespective of the tumor genotype (76% and 83%). The status of the extraserosal invasion and lymph node metastasis (0.691 and 0.802 receiver operating characteristic areas, respectively) predicted by the biopsy genotype and the tumor size corresponded closely to the surgical pathology results. Therefore, the extent of chromosomal losses and the presence of an MSI determined on a biopsy specimen will provide valuable information for making a preoperative genetic diagnosis of a gastric carcinoma.Key words: preoperative genetic diagnosis; gastric carcinoma; chromosomal loss A gastric carcinoma is one of the most common malignancies and leading causes of death. 1 The complete removal (R0) of the residual tumor cells is the only cure, which can be achieved only by a surgical resection of the stomach and locoregional lymph nodes. [2][3][4][5] Clinicians frequently experience several variants of the tumor such as the early nodal involvement of small-sized tumors and the recurrence of early-stage disease. 6,7 This suggests that the metastatic potential varies between cases. In addition, the presence of microscopic tumor cells spreading to the surrounding tissues and distant organs in common cases of gastric carcinoma cannot be predicted from a conventional image and a naked-eye diagnosis. 8 -10 It is believed that genetic instability in a malignancy causes the complex genetic alterations. 11,12 In gastrointestinal carcinomas, a microsatellite instability (MSI) and a loss of heterozygosity (LOH) are frequently observed as a result of the hypermutability of simple repeated nucleotide sequences and unilateral chromosomal losses, respectively. 13,14 The presence of an MSI and the extent (baseline, low, and high levels) of chromosomal losses have been reported t...
The degree of chromosomal losses and the presence of microsatellite instability (MSI) in gastric carcinomas have been categorized into low-risk (low-level loss and MSI) and high-risk (baseline-and high-level losses) genotypes. With the aim of making a preoperative diagnosis, this study confirmed the stem line genotype that is common over an entire tumor as well as in a single biopsy specimen. Biopsy specimens were obtained from 91 gastric carcinoma patients and examined for their microsatellite genotypes using a panel of 41 microsatellite markers on 8 cancer-associated chromosomes. The genotype of the biopsy specimens was compared with that of a surgical specimen, which had been multifocally examined for its intratumoral heterogeneity. Of the 91 pairs of biopsy and surgical specimens, 87 (96%) containing either the same (60 cases) or a similar (17 cases) number of chromosomal losses were categorized into the same microsatellite genotype, and the remaining 4 pairs (4%) were classified into a different genotype. The surgical specimens showed that an extraserosal invasion and lymph node metastasis are frequently associated with either a high-level (4 or more) of chromosomal losses irrespective of the tumor size (73% and 85%) or the large carcinomas > 5 cm in diameter irrespective of the tumor genotype (76% and 83%). The status of the extraserosal invasion and lymph node metastasis (0.691 and 0.802 receiver operating characteristic areas, respectively) predicted by the biopsy genotype and the tumor size corresponded closely to the surgical pathology results. Therefore, the extent of chromosomal losses and the presence of an MSI determined on a biopsy specimen will provide valuable information for making a preoperative genetic diagnosis of a gastric carcinoma.Key words: preoperative genetic diagnosis; gastric carcinoma; chromosomal loss A gastric carcinoma is one of the most common malignancies and leading causes of death. 1 The complete removal (R0) of the residual tumor cells is the only cure, which can be achieved only by a surgical resection of the stomach and locoregional lymph nodes. [2][3][4][5] Clinicians frequently experience several variants of the tumor such as the early nodal involvement of small-sized tumors and the recurrence of early-stage disease. 6,7 This suggests that the metastatic potential varies between cases. In addition, the presence of microscopic tumor cells spreading to the surrounding tissues and distant organs in common cases of gastric carcinoma cannot be predicted from a conventional image and a naked-eye diagnosis. 8 -10 It is believed that genetic instability in a malignancy causes the complex genetic alterations. 11,12 In gastrointestinal carcinomas, a microsatellite instability (MSI) and a loss of heterozygosity (LOH) are frequently observed as a result of the hypermutability of simple repeated nucleotide sequences and unilateral chromosomal losses, respectively. 13,14 The presence of an MSI and the extent (baseline, low, and high levels) of chromosomal losses have been reported t...
2. Mark the correct statement regarding gastric anatomy. Comments The stomach is a rather mobile organ, held in place at either end by the phrenoesophageal ligament proximally and the duodenum distally. This degree of motility allows it to rotate along its axis, creating a gastric volvulus. Gastric volvulus can be organoaxial (i.e., along the longitudinal axis or cascade volvulus along its horizontal axis). The most important predisposing factors are gastric distention and the shape of the stomach itself. Long, vertically oriented stomachs are prone to organoaxial volvulus, whereas broad horizontally oriented stomachs are predisposed to a cascade volvulus. Gastric volvulus has not been associated to gastric banding [ 3 ] (Fig. 12.1 ). Due to its mobility, the stomach is often used to replace the esophagus in the chest. In order to mobilize the stomach, the short gastric vessels, the left gastric artery, the right gastric artery, and the left gastroepiploic artery are divided. In such cases, the right gastroepiploic artery may feed the entire stomach [ 4 ].The stomach is attached to other abdominal organs through the derivatives of the ventral and dorsal mesogastria. The ventral mesogastrium forms the lesser omentum, which may harbor accessory or replaced left hepatic arteries arising from the left gastric artery. The dorsal mesentery forms the gastrosplenic ligament (which encases the short gastric vessels), the splenic capsule, and the splenophrenic ligament [ 5 ]. e) Intrinsic factor is produced by P cells (parietal cells).Comments Gastric acid secretion is the sole function of the parietal cells. This is a fi nely regulated process, under the infl uence of neural, hormonal, and intraluminal stimuli. Parietal cells are located exclusively in the fundus and body of the stomach, which is the basis of limiting highly selective vagotomy to the branches of the nerve of Latarjet going to this portion of the stomach. Located in the antrum, G cells, through gastrin production, are the most important positive regulators of acid secretion. They are stimulated by vagal efferents as well as by the presence of food in the gastric lumen. Gastrin reaches the oxyntic region of the stomach (fundus and body), where it stimulates the production of acid by parietal cells directly and indirectly, by inducing histamine release from enterochromaffi n-like cells. The acidifi cation of the gastric lumen stimulates somatostatin-producing D cells in the antrum, which inhibit G cells in a paracrine manner.Interestingly D cells are also found in the oxyntic region of the stomach; however, in this location, they lack luminal receptors and do not respond to gastric acidifi cation. Instead, they respond to the hormones released by duodenal acidifi cation, namely, CCK, secretin, and gastric inhibitory peptide, and further downregulate gastric production.M cells produce mucus. While they are located throughout the stomach, they are most abundant in the antrum. Chief cells share their location with parietal cells. They produce intrinsic factor,...
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