Differential expression of estrogen receptor-α on follicular dendritic cells from patients with grade 1-2 and grade 3 follicular lymphoma
Differential expression of estrogen receptor-α on follicular dendritic cells from patients with grade 1-2 and grade 3 follicular lymphoma
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DOI:
10.1002/hon.2577
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发表时间:
2019-04-01
影响因子:
3.3
通讯作者:
Yamakawa, Mitsunori
中科院分区:
文献类型:
--
作者:
Ohe, Rintaro;Meng, Hong-Xue;Yamakawa, Mitsunori
Hormone therapy has been used for patients with estrogen receptor alpha (ER alpha)-positive breast cancers. Recently, some studies reported the expression of ER alpha on neoplastic cells from B-cell lymphomas. However, there has been only one report of ER alpha expression on the follicular dendritic cells (FDCs) that structurally and functionally support the microenvironment of follicular lymphomas (FLs). The objective of this study was to investigate the frequency of ER alpha expression on FDCs in nonneoplastic reactive lymphoid tissues and to compare the frequency of ER alpha expression on FDCs in the axillary lymph nodes between patients with and without antiestrogen therapy and among patients with grades 1-3 of FL. Reverse transcription-polymerase chain reaction was performed to detect ER alpha mRNA in FL. In nonneoplastic germinal centers (GCs) from patients with tonsillitis or reactive lymphadenitis, ER alpha was expressed in the light zone. ER alpha-positive cells strongly correlated with the width of GCs (r(s) = 0.81, P < 0.01) and the CD21-positive (r(s) = 0.69, P < 0.01) and CD23-positive (r(s) = 0.83, P < 0.01) FDC meshwork. The axillary lymph nodes had fewer ER alpha-positive cells, smaller GCs, and a looser CD21- and CD23-positive FDC meshwork with hormone therapy than without hormone therapy (P < 0.01). Neoplastic follicles of G1-2 FL had more ER alpha-positive cells and a larger CD23(+) FDC meshwork than those of G3 FL (P < 0.01). ER alpha mRNA was detected in both G1-2 FL and G3 FL by reverse transcription-polymerase chain reaction. In conclusion, these results suggested that antiestrogen hormone therapy may decrease the number of ER alpha-positive FDCs and that the responses mediated by the estrogen-ER alpha interaction on FDCs may differ between G1-2 FL and G3 FL.