ReviewFrontiers in medicine2025
HIF-2α inhibitors in clear cell renal cell carcinoma: a clinical pharmacy perspective on lipid metabolism, therapeutic management, and resistance strategies.
Review in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Drug repurposing of ticagrelor suppresses renal cell carcinoma growth by blockading the EGFR/PI3K/AKT axis.Annals of medicine · 2026Article
- De Novo Lipogenesis in Clear Cell Renal Cell Carcinoma: Mechanistic Insights and Therapeutic Implications.International journal of molecular sciences · 2026Review
- Lipid metabolic reprogramming in clear cell renal cell carcinoma: focus on high-density lipoprotein-related pathways.Oncology reviews · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Renal cell carcinoma (RCC), and clear cell renal cell carcinoma (ccRCC) in particular, is characterized by perturbed lipid metabolism and constitutive activation of hypoxia-inducible factor-2α (HIF-2α). This mini review specifically focuses on ccRCC, which represents 80% of all RCC cases and is uniquely characterized by VHL loss and HIF-2α activation. As a central transcription factor, HIF-2α not only regulates the growth and metastasis of tumor cells but also alters lipid metabolism by activating multiple signaling pathways, thereby promoting tumor progression. Despite the significant advances in our understanding of RCC pathogenesis, there is an urgent need for new targeted therapies. The advance in the design of selective HIF-2α inhibitors has uncovered a novel therapeutic path for ccRCC by direct inhibition of this central oncogenic driver. This mini review outlines how HIF-2α inhibitors exert antitumor effects through specific molecular mechanisms, particularly how they modulate lipid metabolism and related molecular networks. And, the latest clinical trial information is used to determine the effectiveness, safety, and translational potential of the ccRCC as a precision therapy. By integrating existing mechanistic and clinical evidence, the present article intends to instruct the design of future drugs and the optimization of therapeutic modalities so that it might impact the clinical management of ccRCC in the future.
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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 OpenQuestion graph.