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Tissue levels of suppressor of cytokine signaling-3 (SOCS-3) in mycosis fungoides

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AbstractMycosis fungoides (MF) is a type of cutaneous T-cell lymphoma with proposed multifactorial etiology. Suppressor of cytokine signaling-3 (SOCS-3) is one of the proteins expressed in MF. Its exact role in disease pathogenesis has not yet been thoroughly investigated. This study aimed to assess the expression of SOCS-3 in patients’ skin with mycosis fungoides to elucidate their possible role in the pathogenesis in MF. 30 patients with mycosis fungoides and 30 age and sex-matched healthy controls were included. After clinical examination, tissue levels of SOCS-3 were measured by ELISA. The level of expression of SOCS-3 was significantly upregulated in the lesional tissue compared to perilesional SOCS-3 level in patients’ group (P < 0.001), and both levels were higher than the SOCS-3 level in control group (P < 0.001). In addition, there was a statistically significant positive correlation between lesional SOCS-3 level and itching in patients’ group (P < 0.001). Regarding lesional and perilesional SOCS-3 levels in each stage, there was a significant increase in lesional SOCS-3 levels in comparison to perilesional level whether in stage Ia, Ib, and IIa; (P < 0.001), (P < 0.001) and (P < 0.001), respectively. Increased tissue levels of SOCS-3 patients with mycosis fungoides point to a role that SOCS-3 could play in its pathogenesis. Also, high levels of SOCS-3 in MF patients with itching suggest a role in the pathogenesis of this symptom. These findings may prove helpful in formulating a new treatment modality in addition to the current treatment of MF.
Title: Tissue levels of suppressor of cytokine signaling-3 (SOCS-3) in mycosis fungoides
Description:
AbstractMycosis fungoides (MF) is a type of cutaneous T-cell lymphoma with proposed multifactorial etiology.
Suppressor of cytokine signaling-3 (SOCS-3) is one of the proteins expressed in MF.
Its exact role in disease pathogenesis has not yet been thoroughly investigated.
This study aimed to assess the expression of SOCS-3 in patients’ skin with mycosis fungoides to elucidate their possible role in the pathogenesis in MF.
30 patients with mycosis fungoides and 30 age and sex-matched healthy controls were included.
After clinical examination, tissue levels of SOCS-3 were measured by ELISA.
The level of expression of SOCS-3 was significantly upregulated in the lesional tissue compared to perilesional SOCS-3 level in patients’ group (P < 0.
001), and both levels were higher than the SOCS-3 level in control group (P < 0.
001).
In addition, there was a statistically significant positive correlation between lesional SOCS-3 level and itching in patients’ group (P < 0.
001).
Regarding lesional and perilesional SOCS-3 levels in each stage, there was a significant increase in lesional SOCS-3 levels in comparison to perilesional level whether in stage Ia, Ib, and IIa; (P < 0.
001), (P < 0.
001) and (P < 0.
001), respectively.
Increased tissue levels of SOCS-3 patients with mycosis fungoides point to a role that SOCS-3 could play in its pathogenesis.
Also, high levels of SOCS-3 in MF patients with itching suggest a role in the pathogenesis of this symptom.
These findings may prove helpful in formulating a new treatment modality in addition to the current treatment of MF.

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