Chou C Y, Huang S C, Tsai Y C, Hsu K F, Huang K E
Department of Obstetrics and Gynecology, National Cheng Kung University Medical College, Tainan, Taiwan.
Gynecol Oncol. 1997 May;65(2):225-31. doi: 10.1006/gyno.1997.4634.
To investigate the differences of biological aggressiveness in terms of proliferating cell nuclear antigen (PCNA) expression, cell proliferation, and microvessel density between uterine leiomyosarcoma and leiomyoma.
All patients with uterine leiomyosarcoma undergoing surgery at National Cheng Kung University Hospital were eligible. Forty-four patients with uterine myoma were also studied as the benign counterpart. The paraffin-embedded slides were stained with hematoxylin and eosin to confirm the presence of tumor and to quantitate mitoses, PC 10 for measurement of PCNA expression, MIB 1 for measurement of cell proliferation, and factor VIII for quantitation of microvessel density. The immunohistochemical findings of the slides were correlated with clinocopathologic findings of the patients, and the data were analyzed by either chi2 or unpaired t test.
Six patients with uterine leiomyosarcoma and 44 patients with uterine leiomyoma were studied. Statistically significant higher mean levels of PCNA and MIB 1 were observed in uterine leiomyosarcoma compared with those of uterine myoma (for PCNA expression, P = 0.0001; for MIB 1, 11.61 +/- 11.42% vs 0.45 +/- 0.21%, P < 0.0001). No significant difference of microvessel density was observed between these two groups (65.73 +/- 48.62 vs 41.97 +/- 28.20, P = 0.084). Among the six patients with leiomyosarcoma, two patients with a higher percentage of MIB 1-positive tumor cells died of recurrent disease. In contrast, two patients with lower MIB 1 counts were disease-free for 3 years or more.
Deregulated cell growth in uterine leiomyosarcoma may account for the biological aggressiveness of this tumor. Furthermore, the percentage of MIB 1-positive tumor cells seems to be associated with the prognosis or extent of uterine leiomyosarcoma.
探讨子宫平滑肌肉瘤与平滑肌瘤在增殖细胞核抗原(PCNA)表达、细胞增殖及微血管密度方面的生物学侵袭性差异。
国立成功大学医院所有接受手术的子宫平滑肌肉瘤患者均符合条件。44例子宫肌瘤患者作为良性对照也纳入研究。石蜡包埋切片用苏木精和伊红染色以确认肿瘤的存在并定量有丝分裂,用PC10检测PCNA表达,用MIB1检测细胞增殖,用因子VIII定量微血管密度。将切片的免疫组化结果与患者的临床病理结果相关联,并通过卡方检验或不成对t检验分析数据。
研究了6例子宫平滑肌肉瘤患者和44例子宫肌瘤患者。与子宫肌瘤相比,子宫平滑肌肉瘤中PCNA和MIB1的平均水平在统计学上显著更高(PCNA表达,P = 0.0001;MIB1,11.61±11.42%对0.45±0.21%,P < 0.0001)。两组间微血管密度无显著差异(65.73±48.62对41.97±28.20,P = 0.084)。在6例平滑肌肉瘤患者中,2例MIB1阳性肿瘤细胞百分比更高的患者死于复发性疾病。相反,2例MIB1计数较低的患者无病生存3年或更长时间。
子宫平滑肌肉瘤中细胞生长失控可能是该肿瘤生物学侵袭性的原因。此外,MIB1阳性肿瘤细胞的百分比似乎与子宫平滑肌肉瘤的预后或程度相关。