ArticleBMC cancer2025
Multi-omics analysis of bidirectional liquid-liquid phase separation signatures reveals immunotherapy response and prognosis in renal cell carcinoma.
Article in BMC cancer, 2025. 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.
- The role of the WD40-repeat protein family in cancer.Molecular cancer · 2026Review
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
Renal cell carcinoma (RCC) is a common malignant tumor of the urinary system, accounting for approximately 80% of urinary tract malignancies, with clear cell renal cell carcinoma (ccRCC) being the most prevalent subtype. Despite its high incidence, the pathogenesis of ccRCC remains incompletely elucidated, and limitations persist in early diagnosis, targeted therapy, and immunotherapy. Based on emerging evidence highlighting the critical role of liquid-liquid phase separation (LLPS) in tumor proliferation and invasion, this study leveraged multiple ccRCC cohorts to employ Mendelian randomization (MR) and ultimately developed a novel Bidirectional Liquid-Liquid Phase Separation-associated Index (B-LLPSI) using LASSO regression, aiming to predict patient prognosis and therapeutic response. Notably, B-LLPSI demonstrates substantial potential as a universal prognostic indicator across multiple cancer types, underpinning its prospective application in individualized oncology. Paradoxically, while high B-LLPSI levels correlate with poorer patient prognosis, they simultaneously predict enhanced responsiveness to immunotherapy. Furthermore, the B-LLPSI signature was found to be upregulated in tumor tissues and capable of promoting tumor proliferation and invasion. In summary, B-LLPSI holds promise as a robust and independent prognostic tool for diverse cancers, providing critical insights for formulating individualized treatment strategies.
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Registered trials
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