scholarly journals Remodeling the Myeloid Compartment of Triple Negative Breast Cancer by in Situ Immunomodulation

2021 ◽  
Vol 233 (5) ◽  
pp. S29-S30
Author(s):  
Ankit Patel ◽  
Scott I. Abrams ◽  
Fumito Ito
2009 ◽  
Vol 27 (15_suppl) ◽  
pp. 1038-1038
Author(s):  
B. Maiti ◽  
M. N. Kundranda ◽  
T. Jin ◽  
T. P. Spiro ◽  
H. A. Daw

1038 Background: Metabolic syndrome, a conglomerate of obesity, insulin resistance, hypertriglyceridemia, low HDL (high density lipoprotein), and hypertension is associated with an increased risk of breast cancer. However, no clear association has been shown between the highly aggressive triple-negative breast cancer and metabolic syndrome. Methods: In a retrospective review we compared triple-negative and non-triple-negative breast cancer cases for the presence of metabolic syndrome by NCEP (National Cholesterol Education Program) or AACE (American Association of Clinical Endocrinologists) definitions. Data on metabolic syndrome criteria, tumor size, grade, lymph node status, and ductal carcinoma in situ (DCIS) were reviewed. Chi-square test or Student's t-test was used for data analysis. Results: The entire cohort of 176 patients (12.5% African-American) with median age 56.5 years (range 26–91 years) comprised of 86 triple-negative cases and 90 non-triple-negative cases. A statistically significant association of triple-negative breast cancer with metabolic syndrome was observed. According to the NCEP criteria 58.1% of triple negative patients had metabolic syndrome as compared to only 36.7% of non-triple negative patients (p = 0.004). Consistently, by the AACE criteria 52.3% of triple negative patients had metabolic syndrome as compared to 34.4% of non-triple negative patients (p = 0.017). Contrary to blood glucose, triglyceride, or HDL levels, which independently showed significant association with triple-negative breast cancer, hypertension, or BMI showed no independent association. Additionally, triple-negative tumors displayed a significantly higher histologic grade and relative paucity of ductal carcinoma in situ (DCIS) when compared to the non-triple negative tumors (p < 0.001). Conclusions: The data suggests that the metabolic syndrome is significantly more prevalent in triple-negative breast cancer patients when compared to the non-triple-negative patients. Additionally, triple-negative breast cancer showed a significantly higher histologic grade and a relative absence of DCIS. Whether the presence of metabolic syndrome preferentially increases the risk of developing triple-negative-breast cancer needs to be elucidated by future prospective studies. No significant financial relationships to disclose.


2017 ◽  
Vol 65 (6) ◽  
pp. 335-346 ◽  
Author(s):  
Isabelle Bar ◽  
Ahmad Merhi ◽  
Fadi Abdel-Sater ◽  
Abduelhakem Ben Addi ◽  
Sara Sollennita ◽  
...  

The triple-negative breast cancer (TNBC) subtype occurs in about 15% of breast cancer and is an aggressive subtype of breast cancer with poor outcome. Furthermore, treatment of patients with TNBC is more challenging due to the heterogeneity of the disease and the absence of well-defined molecular targets. Microribonucleic acid (RNA) represents a new class of biomarkers that are frequently dysregulated in cancer. It has been described that the microRNA miR-210 is highly expressed in TNBC, and its overexpression had been linked to poor prognosis. TNBC are often infiltrated by immune cells that play a key role in cancer progression. The techniques traditionally used to analyze miR-210 expression such as next generation sequencing or quantitative real-time polymerase chain reaction (PCR) do not allow the precise identification of the cellular subtype expressing the microRNA. In this study, we have analyzed miR-210 expression by in situ hybridization in TNBC. The miR-210 signal was detected in tumor cells, but also in the tumor microenvironment, in a region positive for the pan-leucocyte marker CD45-LCA. Taken together, our results demonstrate that miR-210 is expressed in tumor cells but also in the tumor microenvironment. Our results also highlight the utility of using complementary approaches to take into account the cellular context of microRNA expression.


Nanoscale ◽  
2018 ◽  
Vol 10 (42) ◽  
pp. 19945-19956 ◽  
Author(s):  
Sujuan Sun ◽  
Yunxue Xu ◽  
Peng Fu ◽  
Min Chen ◽  
Suhui Sun ◽  
...  

Enhanced PDT and siRNA transfection effect of siRNA@CpMBs were successfully achieved by in situ conversion of MBs to NPs.


2016 ◽  
Vol 58 (4) ◽  
pp. 283-293
Author(s):  
C. Sebastián Sebastián ◽  
C. García Mur ◽  
S. Cruz Ciria ◽  
D.S. Rosero Cuesta ◽  
B. Gros Bañeres

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