ArticleBlood neoplasia2026
Targeting the G-protein-coupled estrogen receptor: a novel therapeutic strategy in cutaneous T-cell lymphoma.
Article in Blood neoplasia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Corrections and comments
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Authors and funding
19 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cutaneous T-cell lymphoma (CTCL) represents a heterogeneous group of non-Hodgkin lymphomas with limited curative treatment options. The pronounced male predominance in CTCL incidence suggests hormonal influences in disease pathogenesis, prompting investigation into estrogen receptor signaling pathways as therapeutic targets. Building upon previous evidence of tumor-suppressive roles of estrogen signaling via estrogen receptor β, we investigated the therapeutic potential of targeting the G-protein-coupled estrogen receptor (GPER) in CTCL models. We evaluated the antitumor effects of G-1, a selective GPER agonist, in CTCL cell lines and primary patient-derived malignant T cells using in vitro and in vivo approaches. G-1 demonstrated robust dose-dependent cytotoxic effects against CTCL cells, with notable selectivity, as healthy CD4
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.