Authors
Siyu Zhou, Yifan Bi, Ziyi Xiong, Yang Guo, Xiaolu Cui, Mo Zhang
Published in
Critical reviews in oncology/hematology. Pages 105637. Oct 06, 2026. Epub Oct 06, 2026.
Abstract
While immune checkpoint inhibitors (ICIs) have revolutionized the treatment landscape for melanoma and lung cancer, their efficacy in prostate cancer (PCa) remains limited. This therapeutic resistance is linked in part to the "cold" immunophenotype of PCa, which is orchestrated by a highly immunosuppressive tumor microenvironment (TME). Current evidence suggests that distinct spatial barriers and metabolic dysregulation within the TME actively exclude effector lymphocytes and induce exhaustion. Here, we dissect these multidimensional resistance mechanisms, ranging from myeloid cell plasticity to stromal stiffening. We further evaluate how clinical paradigms are shifting from monotherapy to rational combinations, such as those involving poly(ADP-ribose) polymerase (PARP) inhibitors or anti-angiogenic agents, designed to reprogram the TME. Finally, by exploring emerging frontiers including neuroendocrine transdifferentiation, nanobiotechnology, and liquid biopsy, we propose a roadmap for next-generation therapies aimed at sensitizing PCa to immune recognition.
PMID:
42838467
Bibliographic data and abstract were imported from PubMed on 07 Oct 2026.
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