Rubina Kousar

Rubina Kousar


Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
Open access
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BPBbumba Patrick
Bbumba Patrick
TATahira Akhtar
Tahira Akhtar
RKRubina Kousar
Rubina Kousar
Chih-Ching HuangChih-Ching Huang
Chih-Ching Huang
XLXingguo Li
Xingguo Li
Cancer immunotherapy has made breakthrough progress in cancer treatment. However, only a subset of patients benefits from immunotherapy. Given their unique structure, composition, and interactions with the immune system, carbon nanomaterials have recently attracted tremendous interest in their roles as modulators of antitumor immunity. Here, we focused on the latest advances in the immunological effects of carbon nanomaterials. We also reviewed the current preclinical applications of these materials in cancer therapy. Finally, we discussed the challenges to be overcome before the full potential of carbon nanomaterials can be utilized in cancer therapies to ultimately improve patient outcomes.

21 March 2023 in Cells
Verified
Journal Article
Open access
PDF file
TLTimofey Lebedev
Timofey Lebedev
RKRubina Kousar
Rubina Kousar
BPBbumba Patrick
Bbumba Patrick
MUMuhammad Usama
Muhammad Usama
MLMeng-Kuei Lee
Meng-Kuei Lee
XLXingguo Li
Xingguo Li
Epigenetic remodeling and metabolic reprogramming, two well-known cancer hallmarks, are highly intertwined. In addition to their abilities to confer cancer cell growth advantage, these alterations play a critical role in dynamically shaping the tumor microenvironment and antitumor immunity. Recent studies point toward the interplay between epigenetic regulation and metabolic rewiring as a potentially targetable Achilles’ heel in cancer. In this review, we explore the key metabolic mechanisms that underpin the immunomodulatory role of AT-rich interaction domain 1A (ARID1A), the most frequently mutated epigenetic regulator across human cancers. We will summarize the recent advances in targeting ARID1A-deficient cancers by harnessing immune-metabolic vulnerability elicited by ARID1A deficiency to stimulate antitumor immune response, and ultimately, to improve patient outcome.