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Probir Chakravarty

Researcher at Francis Crick Institute

Publications -  101
Citations -  7818

Probir Chakravarty is an academic researcher from Francis Crick Institute. The author has contributed to research in topics: Cancer cell & Tumor microenvironment. The author has an hindex of 37, co-authored 93 publications receiving 5749 citations. Previous affiliations of Probir Chakravarty include National Institutes of Health & Lincoln's Inn.

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NK Cells Stimulate Recruitment of cDC1 into the Tumor Microenvironment Promoting Cancer Immune Control

TL;DR: A cellular and molecular checkpoint for intratumoral cDC1 recruitment is revealed that is targeted by tumor-derived PGE2 for immune evasion and that could be exploited for cancer therapy.
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Cyclooxygenase-Dependent Tumor Growth through Evasion of Immunity

TL;DR: It is shown that the growth of tumors formed by mutant BrafV600E mouse melanoma cells in an immunocompetent host requires their production of prostaglandin E2, which suppresses immunity and fuels tumor-promoting inflammation.
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GM-CSF Mouse Bone Marrow Cultures Comprise a Heterogeneous Population of CD11c(+)MHCII(+) Macrophages and Dendritic Cells.

TL;DR: It is demonstrated that CD11c(+)MHCII(+) BMDCs are in fact a heterogeneous group of cells that comprises conventional DCs and monocyte-derived macrophages, and have important implications for the interpretation of a vast array of data obtained with DC culture systems.
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Interleukin-6 as a Therapeutic Target in Human Ovarian Cancer

TL;DR: In this paper, the authors investigated whether inhibition of IL-6 has therapeutic activity in ovarian cancer via abrogation of a tumor-promoting cytokine network, and they combined pre-clinical and in silico experiments with a phase II clinical trial of the anti-IL-6 antibody siltuximab in patients with platinum-resistant ovarian cancer.
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The tumor-promoting actions of TNF-α involve TNFR1 and IL-17 in ovarian cancer in mice and humans

TL;DR: It is concluded that chronic production of TNF-alpha in the tumor microenvironment increases myeloid cell recruitment in an IL-17-dependent manner that contributes to the tumor-promoting action of this proinflammatory cytokine.