Illustrative Consideration on Factors of Female Genital Cancer Based on Myeongrihak

2019 ◽  
Vol 10 (6) ◽  
pp. 1153-1168
Author(s):  
Jaeseung Lee
1989 ◽  
Vol 42 (8) ◽  
pp. 894-894
Author(s):  
M Wells

1992 ◽  
Vol 7 (1) ◽  
pp. 29-64 ◽  
Author(s):  
W. R. C. M. Weijmar Schultz ◽  
D. D. Bransfield ◽  
H. R. B. M. Van De Wiel ◽  
J. Bouma

1963 ◽  
Vol 18 (1) ◽  
pp. 171-175
Author(s):  
Hervy E. Averette ◽  
Richard C. Hudson ◽  
Manuel I. Viamonte ◽  
Raymond E. Parks ◽  
James H. Ferguson

Cancer ◽  
1962 ◽  
Vol 15 (4) ◽  
pp. 769-775 ◽  
Author(s):  
Hervy E. Averette ◽  
Richard C. Hudson ◽  
Manuel I. Viamonte ◽  
Raymond E. Parks ◽  
James H. Ferguson

BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Pariyada Tanjak ◽  
Bhoom Suktitipat ◽  
Nutchavadee Vorasan ◽  
Panudeth Juengwiwattanakitti ◽  
Benjarat Thiengtrong ◽  
...  

Abstract Background The situation of patients developing multiple primary cancers is becoming more frequent and graver. This study investigated the risks of developing second primary cancers that are related to first primary cancers, and the interval times of synchronous and metachronous multiple primary cancers. Patients and methods Retrospective data were retrieved from 109,054 patients aged ≥18 who were diagnosed with a first solid cancer and registered at Siriraj Cancer Center between 1991 and 2015. A two-month period between first- and second- primary cancers was used to differentiate metachronous and synchronous multiple primary cancers. The combinations of subsequent cancers and relative risks (RRs) of having multiple primary cancers versus having single primary cancer for the top-ten first and second primary cancers were examined. The RR was adjusted for age of the first primary cancer. A survival analysis of the time to second-primary-cancer development was performed. Results Multiple primary cancers were found in 1785 (1.63%) patients. Most (70.87%) second primary cancers occurred after 2 months of first breast, skin, colorectal, lung, head and neck, liver, male genital cancer–prostate, thyroid, and female genital cancer–non-uterine cancers, resulting in those cancers being classified as metachronous multiple primary cancer. After adjustment for age at first diagnosis, head and neck cancers had the highest metachronous association with second esophageal cancers (RR, 25.06; 95% CI, 13.41–50.77). Prostate cancer and second colorectal cancer also demonstrated a high metachronous association (RR, 2.00; 95% CI, 1.25–3.05). A strong synchronous association was found between uterine and ovarian cancers (RR, 27.77; 95% CI, 17.97–43.63). The median time from the first uterine cancer to second-cancer development was 55 days. Conclusions The top-ten most frequent multiple primary cancers were the following: breast; liver; head and neck; colorectal; male genital cancer–prostate; skin; female genital cancer–uterine; thyroid; lung; and female genital cancer–non-uterine. Second primary cancers showed specific associations that depended on the first primary cancer. Physicians should be cognizant of the most common combinations and the interval times of metachronous and synchronous multiple primary cancers.


Author(s):  
A. Petruk ◽  
O. Lytvak ◽  
A. Khabrat

Objective: to review a new potential diagnostic criteria for predictors and premorbid conditions of female genital cancer, including endometrial cancer and breast cancer. Materials and methods. Bibliographic, information-analytical methods were used in the work. Sources of information were data from the scientific literature on the topic of the study, modern gadleins, a review of randomized controlled trials. Results. The results of epidemiological studies suggest that the increased risk of cancer of the female reproductive system is the presence of obesity and type 2 diabetes. Potential mechanisms of their association are hyperinsulinemia, hyperglycemia, chronic inflammation, and insulin resistance. Because insulin is a major regulator of cell metabolism and is a tissue growth factor, hyperinsulinemia increases the risk of cancer. Hyperinsulinemia is associated with increased secretion of androgens by the ovaries and decreased levels of the protein that binds sex hormones, leading to higher concentrations of biologically active estrogens, which are also known to be risk factors for female genital cancer. In recent years, PFAA profiles have been found to be significantly altered in cancer and type 2 diabetes. Because cancer cells require certain amino acids to synthesize DNA, tumor growth factors, build new blood vessels, and duplicate all of their protein content, changes in PFAA profiles can be used as biomarkers of disease and different types of cancer at different stages. Conclusions. With the growing incidence of cancer, the issue of early diagnosis and detection of cancer in the pre-clinical stages remains relevant. Protein metabolism in cancer remains unclear and requires further research using a larger sample size. In addition, the biological mechanisms by which amino acids may contribute to the risk and progression of cancer or other premorbid conditions need to be elucidated. Determining the exact mechanism underlying changes in PFAA profiles has great potential for cancer diagnosis and treatment.


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