Ma Bing, Huang Xiao-Tian, Zou Gui-Jun, Hou Wen-Yu, Du Xiao-Hui
Department of General Surgery, The PLA General Hospital, Beijing 100853, China.
World J Clin Cases. 2022 Jan 14;10(2):469-476. doi: 10.12998/wjcc.v10.i2.469.
A gastric stromal tumor (GST) is a mesenchymal tumor that occurs in the gastrointestinal tract; its biological characteristics are highly complex. Clinically, the severity of a GST is often evaluated by factors such as risk classification, tumor size, and mitotic figures. However, these indicators are not very accurate. Even patients classified as low risk are also at risk of metastasis and recurrence. Therefore, more accurate and objective clinical biological behavior evaluations are urgently needed.
To determine the relationship between Ki-67 and CD44 expression in GSTs and microvessel formation and prognosis.
Eighty-six GST tissue specimens from our hospital were selected for this study. The immunohistochemical staining technique was used to detect Ki-67, CD44, and microvessel density (MVD) in the collected samples to analyze the different risk grades and mitotic figures. In addition, this approach was used to determine the differences in the expression of Ki-67 and CD44 in GST tissues with varying lesion diameters.
In GSTs with positive expression of the Ki-67 protein, the proportions of patients with medium-to-high risk and more than five mitotic counts were 24.07% and 38.89%, respectively. In GSTs with positive expression of the CD44 protein, the proportions of patients with medium-to-high risk and more than five mitotic counts were 23.73% and 38.98%, respectively. In GSTs with negative expression of the Ki-67 protein, these values were relatively high (3.70% and 11.11%, respectively). The MVD in GSTs with positive and negative expression of the CD44 protein was 15.92 ± 2.94 and 13.86 ± 2.98/Hp, respectively; the difference between the two groups was significant ( < 0.05).
Ki-67 and CD44 expression in GSTs is correlated with the grade of tumor risk and mitotic figures. CD44 expression is correlated with microvessel formation in tumor tissues.
胃间质瘤(GST)是一种发生于胃肠道的间叶组织肿瘤,其生物学特性高度复杂。临床上,GST的严重程度常通过风险分级、肿瘤大小和核分裂象等因素进行评估。然而,这些指标并不十分准确。即使是被归类为低风险的患者也存在转移和复发的风险。因此,迫切需要更准确、客观的临床生物学行为评估。
确定胃间质瘤中Ki-67和CD44表达与微血管形成及预后之间的关系。
选取我院86例胃间质瘤组织标本进行本研究。采用免疫组织化学染色技术检测所采集样本中的Ki-67、CD44和微血管密度(MVD),以分析不同风险分级和核分裂象。此外,该方法还用于确定不同病变直径的胃间质瘤组织中Ki-67和CD44表达的差异。
在Ki-67蛋白阳性表达的胃间质瘤中,中高风险及核分裂象超过5个的患者比例分别为24.07%和38.89%。在CD44蛋白阳性表达的胃间质瘤中,中高风险及核分裂象超过5个的患者比例分别为23.73%和38.98%。在Ki-67蛋白阴性表达的胃间质瘤中,这些值相对较高(分别为3.70%和11.11%)。CD44蛋白阳性和阴性表达的胃间质瘤中MVD分别为15.92±2.94和13.86±2.98/Hp;两组间差异有统计学意义(<0.05)。
胃间质瘤中Ki-67和CD44表达与肿瘤风险分级和核分裂象相关。CD44表达与肿瘤组织中的微血管形成相关。