Hypoxia as a driver of resistance to immunotherapy DOI
Joanna Kopecka, Iris C. Salaroglio, Elisabeth Pérez-Ruíz

и другие.

Drug Resistance Updates, Год журнала: 2021, Номер 59, С. 100787 - 100787

Опубликована: Ноя. 18, 2021

Язык: Английский

Targeting macrophages: therapeutic approaches in cancer DOI
Luca Cassetta, Jeffrey W. Pollard

Nature Reviews Drug Discovery, Год журнала: 2018, Номер 17(12), С. 887 - 904

Опубликована: Окт. 26, 2018

Язык: Английский

Процитировано

1604

Hypoxic control of metastasis DOI Open Access
Erinn B. Rankin, Amato J. Giaccia

Science, Год журнала: 2016, Номер 352(6282), С. 175 - 180

Опубликована: Апрель 7, 2016

Metastatic disease is the leading cause of cancer-related deaths and involves critical interactions between tumor cells microenvironment. Hypoxia a potent microenvironmental factor promoting metastatic progression. Clinically, hypoxia expression hypoxia-inducible transcription factors HIF-1 HIF-2 are associated with increased distant metastasis poor survival in variety types. Moreover, HIF signaling malignant influences multiple steps within cascade. Here we review research focused on elucidating mechanisms by which hypoxic microenvironment promotes These studies have identified potential biomarkers therapeutic targets regulated that could be incorporated into strategies aimed at preventing treating disease.

Язык: Английский

Процитировано

1140

Therapeutic Targeting of the Tumor Microenvironment DOI Open Access
Leire Bejarano, Marta Joana Costa Jordão, Johanna A. Joyce

и другие.

Cancer Discovery, Год журнала: 2021, Номер 11(4), С. 933 - 959

Опубликована: Апрель 1, 2021

Abstract Strategies to therapeutically target the tumor microenvironment (TME) have emerged as a promising approach for cancer treatment in recent years due critical roles of TME regulating progression and modulating response standard-of-care therapies. Here, we summarize current knowledge regarding most advanced TME-directed therapies, which either been clinically approved or are currently being evaluated trials, including immunotherapies, antiangiogenic drugs, treatments directed against cancer-associated fibroblasts extracellular matrix. We also discuss some challenges associated with future perspectives this evolving field. Significance: This review provides comprehensive analysis therapies targeting TME, combining discussion underlying basic biology clinical evaluation different therapeutic approaches, highlighting perspectives.

Язык: Английский

Процитировано

1121

Hypoxia induces the breast cancer stem cell phenotype by HIF-dependent and ALKBH5-mediated m 6 A-demethylation of NANOG mRNA DOI Open Access
Chuanzhao Zhang,

Debangshu Samanta,

Haiquan Lu

и другие.

Proceedings of the National Academy of Sciences, Год журнала: 2016, Номер 113(14)

Опубликована: Март 21, 2016

Significance Pluripotency factors, such as NANOG, play a critical role in the maintenance and specification of cancer stem cells, which are required for primary tumor formation metastasis. In this study, we report that exposure breast cells to hypoxia (i.e., reduced O 2 availability), is feature microenvironment, induces N 6 -methyladenosine (m A) demethylation stabilization NANOG mRNA, thereby promoting cell (BCSC) phenotype. We show inhibiting expression AlkB homolog 5 (ALKBH5), demethylates m A, or hypoxia-inducible factors (HIFs) HIF-1α HIF-2α, activate ALKBH5 gene transcription hypoxic an effective strategy decrease target BCSCs vivo.

Язык: Английский

Процитировано

890

Hypoxia-Inducible Factors: Master Regulators of Cancer Progression DOI Creative Commons
Luana Schito, Gregg L. Semenza

Trends in cancer, Год журнала: 2016, Номер 2(12), С. 758 - 770

Опубликована: Ноя. 17, 2016

Язык: Английский

Процитировано

806

Phagocytosis checkpoints as new targets for cancer immunotherapy DOI
Mingye Feng, Wen Jiang, Betty Y.S. Kim

и другие.

Nature reviews. Cancer, Год журнала: 2019, Номер 19(10), С. 568 - 586

Опубликована: Авг. 28, 2019

Язык: Английский

Процитировано

765

The Role of HIF in Immunity and Inflammation DOI Creative Commons
Anne F. McGettrick, Luke O'neill

Cell Metabolism, Год журнала: 2020, Номер 32(4), С. 524 - 536

Опубликована: Авг. 26, 2020

Язык: Английский

Процитировано

513

Cancer Stem Cells: The Architects of the Tumor Ecosystem DOI Creative Commons
Briana C. Prager, Qi Xie, Shideng Bao

и другие.

Cell stem cell, Год журнала: 2019, Номер 24(1), С. 41 - 53

Опубликована: Янв. 1, 2019

Язык: Английский

Процитировано

500

The CD47-SIRPα Immune Checkpoint DOI Creative Commons
Meike E. W. Logtenberg, Ferenc A. Scheeren, Ton N. Schumacher

и другие.

Immunity, Год журнала: 2020, Номер 52(5), С. 742 - 752

Опубликована: Май 1, 2020

Язык: Английский

Процитировано

471

The CD47‐SIRPα signaling axis as an innate immune checkpoint in cancer DOI

Hanke L. Matlung,

Katka Szilagyi,

Neil Barclay

и другие.

Immunological Reviews, Год журнала: 2017, Номер 276(1), С. 145 - 164

Опубликована: Март 1, 2017

Summary Immune checkpoint inhibitors, including those targeting CTLA ‐4/B7 and the PD ‐1/ ‐L1 inhibitory pathways, are now available for clinical use in cancer patients, with other interesting inhibitors being currently development. Most of these have purpose to promote adaptive T cell‐mediated immunity against cancer. Here, we review another acting potentiate activity innate immune cells towards This is composed what has become known as ‘don't‐eat me’ signal CD 47, which a protein broadly expressed on normal often overexpressed cells, its counter‐receptor, myeloid immunoreceptor SIRP α. Blocking 47‐ α interactions been shown destruction by phagocytes, macrophages neutrophils. Furthermore, there growing evidence that axis may also antigen‐presenting cell function thereby stimulate anti‐cancer immunity. The development potential side effects discussed. Collectively, this identifies promising cancer, data first studies expected within coming years, an exciting rapidly developing field.

Язык: Английский

Процитировано

457