Clinicopathological assessment of cancer/testis antigens NY‑ESO‑1 and MAGE‑A4 in osteosarcoma.

IF 2.1 4区 生物学 Q4 CELL BIOLOGY
Kazuhiko Hashimoto, Shunji Nishimura, Tomohiko Ito, Naohiro Oka, Ryosuke Kakinoki, Masao Akagi
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引用次数: 0

Abstract

The cancer/testis antigens (CTAs), New York esophageal squamous cell carcinoma-1 (NY-ESO-1) and melanoma antigen gene (MAGE)-A4 are normally restricted to male germ cells but are aberrantly expressed in several cancers. Considering the limited information regarding their significance in osteosarcoma (OS), the purpose of this study was to determine the clinical significance of NY-ESO-1 and MAGE-A4 expression in OS. Nine patients with OS treated at Kindai University Hospital were included in the study. The median age was 27 years, and median follow-up period was 40 months. The specimens obtained at the time of biopsy were used to perform immunostaining for NY-ESO, MAGE-A4, p53, and Ki-67. The positive cell rates and positive case rates of NY-ESO, MAGE-A4, p53, and Ki-67 were calculated. The correlation between the positive cell rate of immunohistochemical markers was also calculated. The correlation between the positive cell rate of NY-ESO-1 or MAGE-A4 and tumor size or maximum standardized uptake (SUV-max) was also determined. The positive cell rates of NY-ESO-1 or MAGE-A4 in continuous disease-free (CDF) cases were also compared with those in alive with disease (AWD) or dead of disease (DOD) cases. The average positive cell rates of NY-ESO, MAGEA4, p53, and Ki-67 were 71.7%, 85.1%, 16.2%, and 14.7%, and their positive case rates were 33.3%, 100%, 44.4%, and 100%, respectively. The positivity rates of NY-ESO-1 and p53 were strongly correlated, whereas those of NY-ESO-1 and Ki-67 were moderately correlated. The MAGE-A4 and p53 positivity rates and the MAGE-A4 and Ki-67 positive cell rates were both strongly correlated. The NY-ESO-1 and MAGE-A4 positivity rates were moderately correlated. The positive correlation between the NY-ESO-1 positive cell rate and tumor size was medium, and that between the MAGE-A4 positivity rate and SUV-max was very strong. There was no significant difference in the positive cell rates of NY-ESO-1 or MAGE-A4 between CDF cases and AWD or DOD cases. Overall, our results suggest that NY-ESO-1 and MAGE-A4 may be involved in the aggressiveness of OS.

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骨肉瘤中癌症/睾丸抗原 NY-ESO-1 和 MAGE-A4 的临床病理评估。
癌症/睾丸抗原(CTA)、纽约食管鳞状细胞癌-1(NY-ESO-1)和黑色素瘤抗原基因(MAGE)-A4通常仅限于男性生殖细胞,但在多种癌症中异常表达。考虑到有关它们在骨肉瘤(OS)中重要性的信息有限,本研究旨在确定 NY-ESO-1 和 MAGE-A4 表达在 OS 中的临床意义。研究纳入了在金台大学医院接受治疗的九名骨肉瘤患者。中位年龄为27岁,中位随访时间为40个月。活检时获得的标本用于对 NY-ESO、MAGE-A4、p53 和 Ki-67 进行免疫染色。计算了NY-ESO、MAGE-A4、p53和Ki-67的阳性细胞率和阳性病例率。还计算了免疫组化标记物阳性细胞率之间的相关性。还确定了 NY-ESO-1 或 MAGE-A4 阳性细胞率与肿瘤大小或最大标准化摄取量(SUV-max)之间的相关性。连续无病(CDF)病例的 NY-ESO-1 或 MAGE-A4 阳性率也与带病生存(AWD)或病死(DOD)病例进行了比较。NY-ESO、MAGEA4、p53和Ki-67的平均阳性细胞率分别为71.7%、85.1%、16.2%和14.7%,阳性病例率分别为33.3%、100%、44.4%和100%。NY-ESO-1和p53的阳性率呈强相关,而NY-ESO-1和Ki-67的阳性率呈中度相关。MAGE-A4和p53阳性率以及MAGE-A4和Ki-67阳性细胞率均呈强相关。NY-ESO-1 和 MAGE-A4 阳性率呈中度相关。NY-ESO-1阳性细胞率与肿瘤大小呈中度正相关,MAGE-A4阳性细胞率与SUV-max呈高度正相关。CDF病例与AWD或DOD病例的NY-ESO-1或MAGE-A4阳性细胞率无明显差异。总之,我们的研究结果表明,NY-ESO-1和MAGE-A4可能与OS的侵袭性有关。
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来源期刊
European Journal of Histochemistry
European Journal of Histochemistry 生物-细胞生物学
CiteScore
3.70
自引率
5.00%
发文量
47
审稿时长
3 months
期刊介绍: The Journal publishes original papers concerning investigations by histochemical and immunohistochemical methods, and performed with the aid of light, super-resolution and electron microscopy, cytometry and imaging techniques. Coverage extends to: functional cell and tissue biology in animals and plants; cell differentiation and death; cell-cell interaction and molecular trafficking; biology of cell development and senescence; nerve and muscle cell biology; cellular basis of diseases. The histochemical approach is nowadays essentially aimed at locating molecules in the very place where they exert their biological roles, and at describing dynamically specific chemical activities in living cells. Basic research on cell functional organization is essential for understanding the mechanisms underlying major biological processes such as differentiation, the control of tissue homeostasis, and the regulation of normal and tumor cell growth. Even more than in the past, the European Journal of Histochemistry, as a journal of functional cytology, represents the venue where cell scientists may present and discuss their original results, technical improvements and theories.
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