Abstract:Reproductive history and exogenous hormonal exposures are acknowledged risk factors for breast cancer in the general population. In women at increased breast cancer risk for genetic predisposition or positive family history, data regarding these risk factors are limited or conflicting, and recommendations for these categories are unclear. We evaluated the characteristics of reproductive life in 2522 women at increased genetic or familial breast cancer risk attending our Family Cancer Center. Breast cancers in … Show more
“…This is supported by Lambertini et al study (17) which confirmed the protective effect of ever breastfeeding against hormone receptor-negative breast cancer, which is more common in younger women. Also, Toss et al (18) found a protective effect of breastfeeding only in triple negative breast cancer which represent only 15% of breast cancer cases and this explains the results of the present study which found that breastfeeding had no protective effect against familial breast cancer.…”
Section: Resultssupporting
confidence: 61%
“…The same finding was reported by results of several studies. (17,18,20) Horn et al (21) explained this finding by the fact that familial breast cancer is more frequently hormone receptor negative tumors, while age at menarche, age at first delivery and parity seems to modify mostly the incidence of hormone receptor-positive tumors.…”
Background: Breast cancer is the most common female malignancy. The family history of breast cancer increases the risk of the disease. Objectives: To assess the frequency of familial breast cancer among breast cancer patients attending oncology outpatient clinics in Menoufia University Hospital and to compare the clinical and pathological characteristics of familial and sporadic breast cancer. Methods: The study was conducted on 150 women with familial or sporadic breast cancer who were attending oncology outpatient clinics, Menoufia University Hospital for follow up or receiving treatment. The participants were interviewed by predesigned questionnaire to assess risk factors for breast cancer. Data on different characteristics of the tumors were gathered from patients' medical records. Results: Familial cases represented 18.7% of studied breast cancer patients. The age of onset seems to be younger in familial breast cancers (P=0.008). Percentage of familial breast cancer cases was significantly more prevalent among premenopausal females (P=0.007). Percentage of studied cases who breastfed their babies, had bilateral breast cancer, had triple negative breast cancer and with larger tumor size (T4) was significantly more prevalent among familial than sporadic breast cancer cases (P=0.023, 0.006, 0.000, 0.000 respectively). About 63% of sporadic cases were among hormonal contraceptive users versus 43% in familial group (P=0.040). There was no significant difference between familial and sporadic groups regarding histological type was observed. Conclusion: Familial cases represented 18.7% of studied breast cancer patients. Familial breast cancer seems to affect premenopausal young women and tends to present at the larger size, bilateral and triple negative tumors.
“…This is supported by Lambertini et al study (17) which confirmed the protective effect of ever breastfeeding against hormone receptor-negative breast cancer, which is more common in younger women. Also, Toss et al (18) found a protective effect of breastfeeding only in triple negative breast cancer which represent only 15% of breast cancer cases and this explains the results of the present study which found that breastfeeding had no protective effect against familial breast cancer.…”
Section: Resultssupporting
confidence: 61%
“…The same finding was reported by results of several studies. (17,18,20) Horn et al (21) explained this finding by the fact that familial breast cancer is more frequently hormone receptor negative tumors, while age at menarche, age at first delivery and parity seems to modify mostly the incidence of hormone receptor-positive tumors.…”
Background: Breast cancer is the most common female malignancy. The family history of breast cancer increases the risk of the disease. Objectives: To assess the frequency of familial breast cancer among breast cancer patients attending oncology outpatient clinics in Menoufia University Hospital and to compare the clinical and pathological characteristics of familial and sporadic breast cancer. Methods: The study was conducted on 150 women with familial or sporadic breast cancer who were attending oncology outpatient clinics, Menoufia University Hospital for follow up or receiving treatment. The participants were interviewed by predesigned questionnaire to assess risk factors for breast cancer. Data on different characteristics of the tumors were gathered from patients' medical records. Results: Familial cases represented 18.7% of studied breast cancer patients. The age of onset seems to be younger in familial breast cancers (P=0.008). Percentage of familial breast cancer cases was significantly more prevalent among premenopausal females (P=0.007). Percentage of studied cases who breastfed their babies, had bilateral breast cancer, had triple negative breast cancer and with larger tumor size (T4) was significantly more prevalent among familial than sporadic breast cancer cases (P=0.023, 0.006, 0.000, 0.000 respectively). About 63% of sporadic cases were among hormonal contraceptive users versus 43% in familial group (P=0.040). There was no significant difference between familial and sporadic groups regarding histological type was observed. Conclusion: Familial cases represented 18.7% of studied breast cancer patients. Familial breast cancer seems to affect premenopausal young women and tends to present at the larger size, bilateral and triple negative tumors.
“…Despite the availability of new biological drugs and a more rational use of therapies, the clinical outcome remains poor. Thus, the life expectancy of patients with advanced disease is dismal, and the median survival of a mixed population of metastatic breast cancer patients has not substantially improved in the last decades (Chia et al 2007, Dawood et al 2008, Welt et al 2016, Toss et al 2017.…”
Section: Probable Reasons For the Discrepancy Between Genetic And Biomentioning
It has become clearer that advanced cancer, especially advanced breast cancer, is an entirely displayed pathological system that is much more complex than previously considered. However, the direct relationship between tumour growth and immune evasion can represent a general rule governing the pathological cancer system from the initial cancer cells to when the system is entirely displayed. Accordingly, a refined pathobiological model and a novel therapeutic strategy are proposed. The novel therapeutic strategy is based on therapeutically induced conditions (undetectable tumour burden and/or a prolonged tumour 'resting state'), which enable an efficacious immune response in advanced breast and other types of solid cancers.
“…Various factors play a role in breast cancer mutagenesis including gene mutations, prolonged endogenous and exogenous estrogen exposure, and family history. 32 Despite the advancements in cancer management, therapies that increase the survival rate while improving life quality of patients are still required. 33 As it avoids systemic adverse effects by exerting a local response and being capable of initiating antitumor immunity, PDT may be an attractive option for breast cancer treatment; both alone and in combination with other procedures.…”
In
this study, we synthesized and characterized a silicon phthalocyanine
substituted with 3-hydroxypyridin-2-thione (
SiPc-HDACi
), designed to be a chemophotodynamic therapy agent acting as a histone
deacetylase inhibitor, and we determined its photophysical, photochemical,
and photobiological properties. Next, we evaluated its anticancer
efficacy on MCF-7, double positive and MDA-MB-231, triple negative
breast cancer cell lines, as well as on a healthy human endothelial
cell line (HUVEC). Our results indicate that
SiPc-HDACi
can target nucleoli of cells, effectively inducing apoptosis while
promoting cell cycle arrest thanks to its high singlet oxygen yield
and its histone deacetylase downregulating properties, suggesting
a powerful anticancer effect on breast cancer
in vitro
. Our further studies will be conducted with primary breast cancer
cell culture to give a better insight into the anticancer mechanism
of the compound.
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