Zareifar Soheila, Ghorbani Soudeh, Monabbati Ahmad, Bordbar Mohammad Reza, Zekavat Omid Reza, Abdolkarimi Babak, Haghpanah Sezaneh
a Hematology Research Center , Shiraz University of Medical Sciences , Shiraz , Iran.
b Department of Pathology and Hematopathology research center , Shiraz University of Medical Sciences , Shiraz , Iran.
Pediatr Hematol Oncol. 2018 May;35(4):250-256. doi: 10.1080/08880018.2018.1530702. Epub 2018 Dec 27.
Survivin and livin are highly expressed in various malignancies and their expression levels may be related to unfavorable prognosis. The aim was to investigate the relationships of these two markers with some prognostic factors and with survival of the children with acute myeloid leukemia (AML).
Livin and survivin expression was investigated quantitatively by immunohistochemistry staining technique in 43 primary formalin-fixed, paraffin-embedded bone marrow blocks in pediatric age group (<18 years).
Both survivin and livin were expressed in 81.4% of AML patients. Livin expression showed significant positive association with high level of primary WBC (p = .002). Survivin expression showed significant positive correlations with risk of relapse (p ≤ .001) and high level of primary WBC (p = .003). The relationship of overall survival (OS) of the patients with livin and survivin expression, were investigated separately in disease subtypes. Significant association was observed between survivin expression and shorter OS regardless of subtypes including acute promyelocytic (APL) (p = .01) and nonacute promyelocytic leukemia (non-APL) (p = .008). Also, significant association of livin expression with shorter OS was detected, but only in APL subgroup (p = .046). Nevertheless, in Cox regression model after adjusting for disease subtypes, stage and cytogenetics; survivin and livin showed no significant association with OS (p > .05).
Livin and survivin showed significant associations with some poor prognostic factors of AML. Although survivin in both subtypes and livin in non APL subtype, showed a significant relationship with shorter OS, none of them was determined as independent prognostic factors. Further studies with larger sample size are suggested.
Survivin和Livin在多种恶性肿瘤中高表达,其表达水平可能与不良预后相关。本研究旨在探讨这两种标志物与急性髓系白血病(AML)患儿的一些预后因素及生存率之间的关系。
采用免疫组织化学染色技术对43例年龄小于18岁儿童的原发性福尔马林固定、石蜡包埋骨髓块中Livin和Survivin的表达进行定量研究。
81.4%的AML患者同时表达Survivin和Livin。Livin表达与初诊时白细胞高水平呈显著正相关(p = 0.002)。Survivin表达与复发风险(p≤0.001)和初诊时白细胞高水平(p = 0.003)呈显著正相关。分别在疾病亚型中研究了Livin和Survivin表达与患者总生存期(OS)的关系。无论亚型如何,包括急性早幼粒细胞白血病(APL)(p = 0.01)和非急性早幼粒细胞白血病(非APL)(p = 0.008),Survivin表达与较短的OS之间均存在显著相关性。此外,Livin表达与较短的OS也存在显著相关性,但仅在APL亚组中(p = 0.046)。然而,在调整疾病亚型、分期和细胞遗传学因素后的Cox回归模型中,Survivin和Livin与OS均无显著相关性(p>0.05)。
Livin和Survivin与AML的一些不良预后因素显著相关。虽然Survivin在两种亚型中以及Livin在非APL亚型中均与较短的OS存在显著关系,但它们均未被确定为独立的预后因素。建议进行更大样本量的进一步研究。