Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2026
Stromal Expression of TNF-α and Its Receptors TNFR1 and TNFR2: Association with Blood Count Parameters in Ovarian Cancer.
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Nomelini Rosekeila Simões, Sanguinete Marcela Moisés Maluf, Modesto Clícia Chagas, Cruz Fabrícia Fernanda Barros, Amaral Neila Caroline Alves, Jammal Millena Prata, Côbo Eliângela de Castro, Etchebehere Renata Margarida, Murta Eddie Fernando Candido
Аннотация
The objective of this study was to evaluate the association between immunostaining of tumor necrosis factor-alpha (TNF-α) and its receptors in the stroma of malignant ovarian neoplasm with hemogram parameters and tumor markers. Women with a confirmed diagnosis of malignant or borderline ovarian neoplasm were included (n = 43). Age, hormonal status, histological type, histological grade, staging, type of carcinogenesis, and blood count parameters were recorded. For the immunohistochemical study, TNF-α and its receptors were evaluated in peritumoral stroma. Receiver operating characteristic curve and multivariate analysis were performed. The level of significance was <0.05. For TNF-α, there was statistical significance for basophils (cutoff value >0) and neutrophils (cutoff value ≤3,900) between strong and weak immunostaining. In relation to TNF-α receptor 1 (TNFR1), a cutoff value of monocytes >312 per mm3 was found. Regarding TNF-α receptor 2 (TNFR2), the cutoff value of CA-125 was ≤95.16 U/mL. Still regarding TNFR2, the cutoff value for the absolute platelet count was ≤298,000 per mm3. Multivariate analysis showed that an absolute monocyte count >312 per mm3 is associated with strong stromal immunostaining of TNFR1, and a platelet count ≤298,000 per mm3 is associated with strong stromal immunostaining of TNFR2. Therefore, an absolute monocyte count >312 per mm3 is associated with strong stromal immunostaining of TNFR1, and a platelet count ≤298,000 per mm3 is associated with strong stromal immunostaining of TNFR2.