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Breast cancer chemotherapy induces vascular dysfunction and hypertension through a NOX4-dependent mechanism
Piotr Szczepaniak, … , David G. Harrison, Tomasz J. Guzik
Piotr Szczepaniak, … , David G. Harrison, Tomasz J. Guzik
Published May 26, 2022
Citation Information: J Clin Invest. 2022;132(13):e149117. https://doi.org/10.1172/JCI149117.
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Research Article Vascular biology

Breast cancer chemotherapy induces vascular dysfunction and hypertension through a NOX4-dependent mechanism

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Abstract

Cardiovascular disease is the major cause of morbidity and mortality in breast cancer survivors. Chemotherapy contributes to this risk. We aimed to define the mechanisms of long-term vascular dysfunction caused by neoadjuvant chemotherapy (NACT) and identify novel therapeutic targets. We studied arteries from postmenopausal women who had undergone breast cancer treatment using docetaxel, doxorubicin, and cyclophosphamide (NACT) and from women with no history of such treatment matched for key clinical parameters. We explored mechanisms in WT and Nox4–/– mice and in human microvascular endothelial cells. Endothelium-dependent, NO-mediated vasodilatation was severely impaired in patients after NACT, while endothelium-independent responses remained normal. This was mimicked by a 24-hour exposure of arteries to NACT agents ex vivo. When applied individually, only docetaxel impaired endothelial function in human vessels. Mechanistic studies showed that NACT increased inhibitory eNOS phosphorylation of threonine 495 in a Rho-associated protein kinase–dependent (ROCK-dependent) manner and augmented vascular superoxide and hydrogen peroxide production and NADPH oxidase activity. Docetaxel increased expression of the NADPH oxidase NOX4 in endothelial and smooth muscle cells and NOX2 in the endothelium. A NOX4 increase in human arteries may be mediated epigenetically by diminished DNA methylation of the NOX4 promoter. Docetaxel induced endothelial dysfunction and hypertension in mice, and these were prevented in Nox4–/– mice and by pharmacological inhibition of Nox4 or Rock. Commonly used chemotherapeutic agents and, in particular, docetaxel alter vascular function by promoting the inhibitory phosphorylation of eNOS and enhancing ROS production by NADPH oxidases.

Authors

Piotr Szczepaniak, Mateusz Siedlinski, Diana Hodorowicz-Zaniewska, Ryszard Nosalski, Tomasz P. Mikolajczyk, Aneta M. Dobosz, Anna Dikalova, Sergey Dikalov, Joanna Streb, Katarzyna Gara, Pawel Basta, Jaroslaw Krolczyk, Joanna Sulicka-Grodzicka, Ewelina Jozefczuk, Anna Dziewulska, Blessy Saju, Iwona Laksa, Wei Chen, John Dormer, Maciej Tomaszewski, Pasquale Maffia, Marta Czesnikiewicz-Guzik, Filippo Crea, Agnieszka Dobrzyn, Javid Moslehi, Tomasz Grodzicki, David G. Harrison, Tomasz J. Guzik

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Figure 2

Effects of breast cancer neoadjuvant chemotherapy using docetaxel, cyclophosphamide, and doxorubicin (NACT) on the regulation of eNOS.

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Effects of breast cancer neoadjuvant chemotherapy using docetaxel, cyclo...
(A) Endothelium-dependent vasorelaxation responses to ACh (1 nM to 10 μM) in arteries from patients without NACT and from patients with prior NACT after preincubation with l-NAME (100 μM) (n = 8/group). Data expressed as the mean ± SEM. ***P < 0.001 versus no NACT; *P < 0.05 versus no NACT; 2-way, repeated-measures ANOVA with Tukey’s test. (B) Expression of eNOS mRNA (n = 13–16/group; bottom left) and eNOS protein (Western blotting; n = 12/group) in arteries from patients without NACT and from patients who underwent NACT. (C) Phosphorylation of eNOS at Ser1177 (left; n = 12/group) and at Thr495 in arteries from patients with or without prior NACT (right; n = 12/group), normalized to total eNOS. Data were derived from 3 independent experiments and are expressed as the mean ± SEM. ****P < 0.0001 versus no NACT; 2-tailed, unpaired Student’s t test. (D) Effects of in vivo exposure to docetaxel in C57BL/6J mice (i.p. injections; 10 mg/kg or placebo every 5 days for 3 weeks) on the inhibitory phosphorylation of eNos at Thr495, normalized to total eNOS in mouse aortas (n = 5 mice/group). Data are expressed as the mean ± SEM. **P < 0.01 versus WT; 2-tailed, unpaired Student’s t test. (E) Rho kinase activity in arteries from patients with or without NACT (n = 10/group; left) and in HDMECs (n = 5/group; right). Data are expressed as the mean ± SEM. ***P < 0.001 versus vehicle or no NACT; 2-tailed, unpaired Student’s t test. (F) Effects of docetaxel (100 nM) on eNOS at Thr495 phosphorylation in HDMECs and the modulating effect of docetaxel plus Go6976 (1 μM) or docetaxel plus Y27632 (5 μM) (n = 6/group). Densitometric analysis of proteins normalized to total eNOS is shown. Immunoblots are from 1 of 2 independent experiments (left) and are expressed as the mean ± SEM. **P < 0.01 versus vehicle or docetaxel; *P < 0.05 versus docetaxel; 1-way ANOVA with Tukey’s test.

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