In Vivo Imaging of Pressure Effects in Normal Breast Tissue with Quantitative Multi-Spectral Near-Infrared Tomography

Author(s):  
Shudong Jiang ◽  
Brian W. Pogue ◽  
Xiaomei Song ◽  
Subhadra Srinivasan ◽  
Keith D. Paulsen ◽  
...  
2005 ◽  
Vol 10 (5) ◽  
pp. 051704 ◽  
Author(s):  
Xin Wang ◽  
Brian W. Pogue ◽  
Shudong Jiang ◽  
Xiaomei Song ◽  
Keith D. Paulsen ◽  
...  

2020 ◽  
Vol 105 (5) ◽  
pp. 1617-1628 ◽  
Author(s):  
Nina Dabrosin ◽  
Charlotta Dabrosin

Abstract Context Dense breast tissue is associated with 4 to 6 times higher risk of breast cancer by poorly understood mechanisms. No preventive therapy for this high-risk group is available. After menopause, breast density decreases due to involution of the mammary gland. In dense breast tissue, this process is haltered by undetermined biological actions. Growth hormone (GH) and insulin-like binding proteins (IGFBPs) play major roles in normal mammary gland development, but their roles in maintaining breast density are unknown. Objective To reveal in vivo levels of GH, IGFBPs, and other pro-tumorigenic proteins in the extracellular microenvironment in breast cancer, in normal breast tissue with various breast density in postmenopausal women, and premenopausal breasts. We also sought to determine possible correlations between these determinants. Setting and Design Microdialysis was used to collect extracellular in vivo proteins intratumorally from breast cancers before surgery and from normal human breast tissue from premenopausal women and postmenopausal women with mammographic dense or nondense breasts. Results Estrogen receptor positive breast cancers exhibited increased extracellular GH (P < .01). Dense breasts of postmenopausal women exhibited similar levels of GH as premenopausal breasts and significantly higher levels than in nondense breasts (P < .001). Similar results were found for IGFBP-1, -2, -3, and -7 (P < .01) and for IGFBP-6 (P <.05). Strong positive correlations were revealed between GH and IGFBPs and pro-tumorigenic matrix metalloproteinases, urokinase-type plasminogen activator, Interleukin 6, Interleukin 8, and vascular endothelial growth factor in normal breast tissue. Conclusions GH pathways may be targetable for cancer prevention therapeutics in postmenopausal women with dense breast tissue.


2007 ◽  
Vol 9 (8) ◽  
pp. 1143-1156 ◽  
Author(s):  
Subhadra Srinivasan ◽  
Brian W. Pogue ◽  
Colin Carpenter ◽  
Shudong Jiang ◽  
Wendy A. Wells ◽  
...  

2016 ◽  
Vol 21 (9) ◽  
pp. 091316 ◽  
Author(s):  
Kelly E. Michaelsen ◽  
Venkataramanan Krishnaswamy ◽  
Linxi Shi ◽  
Srinivasan Vedantham ◽  
Andrew Karellas ◽  
...  

2009 ◽  
Vol 48 (10) ◽  
pp. D130 ◽  
Author(s):  
Shudong Jiang ◽  
Brian W. Pogue ◽  
Ashley M. Laughney ◽  
Christine A. Kogel ◽  
Keith D. Paulsen

Cancers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 891 ◽  
Author(s):  
Ninna C. S. Voss ◽  
Thomas Dreyer ◽  
Mikkel B. Henningsen ◽  
Pernille Vahl ◽  
Bent Honoré ◽  
...  

The acidic tumor microenvironment modifies malignant cell behavior. Here, we study consequences of the microenvironment in breast carcinomas. Beginning at carcinogen-based breast cancer induction, we supply either regular or NaHCO3-containing drinking water to female C57BL/6j mice. We evaluate urine and blood acid-base status, tumor metabolism (microdialysis sampling), and tumor pH (pH-sensitive microelectrodes) in vivo. Based on freshly isolated epithelial organoids from breast carcinomas and normal breast tissue, we assess protein expression (immunoblotting, mass spectrometry), intracellular pH (fluorescence microscopy), and cell proliferation (bromodeoxyuridine incorporation). Oral NaHCO3 therapy increases breast tumor pH in vivo from 6.68 ± 0.04 to 7.04 ± 0.09 and intracellular pH in breast epithelial organoids by ~0.15. Breast tumors develop with median latency of 85.5 ± 8.2 days in NaHCO3-treated mice vs. 82 ± 7.5 days in control mice. Oral NaHCO3 therapy does not affect tumor growth, histopathology or glycolytic metabolism. The capacity for cellular net acid extrusion is increased in NaHCO3-treated mice and correlates negatively with breast tumor latency. Oral NaHCO3 therapy elevates proliferative activity in organoids from breast carcinomas. Changes in protein expression patterns—observed by high-throughput proteomics analyses—between cancer and normal breast tissue and in response to oral NaHCO3 therapy reveal complex influences on metabolism, cytoskeleton, cell-cell and cell-matrix interaction, and cell signaling pathways. We conclude that oral NaHCO3 therapy neutralizes the microenvironment of breast carcinomas, elevates the cellular net acid extrusion capacity, and accelerates proliferation without net effect on breast cancer development or tumor growth. We demonstrate unexpected pro-neoplastic consequences of oral NaHCO3 therapy that in breast tissue cancel out previously reported anti-neoplastic effects.


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