A highly sensitive aptasensor for the detection of prostate specific antigen based on dumbbell hybridization chain reaction

2021 ◽  
Vol 340 ◽  
pp. 129952
Author(s):  
Yu Jiang ◽  
Xifeng Chen ◽  
Ninghan Feng ◽  
Peng Miao
1996 ◽  
Vol 42 (3) ◽  
pp. 361-366 ◽  
Author(s):  
N Zarghami ◽  
E P Diamandis

Abstract We have developed reverse transcription-polymerase chain reaction (RT- PCR) methods for detecting prostate-specific antigen (PSA) mRNA. Using these methods, and a highly sensitive immunofluorometric assay for measuring PSA protein, we have assessed the concentrations of PSA mRNA and PSA protein in 30 primary breast tumors and a few other control tissues. We found good agreement between presence of PSA protein and PSA mRNA in breast tumors. We thus propose that, in women, detection of PSA protein or PSA mRNA in tissues and tumors offers equivalent information. Because PSA protein is present in male blood and thus could contaminate extracts from tumors and tissues from men, we propose that the RT-PCR methods we describe be used to assess nonprostatic expression of the PSA gene in men.


2020 ◽  
Vol 92 (5) ◽  
pp. 4046-4052 ◽  
Author(s):  
Jia Ru Wang ◽  
Chang Xia ◽  
Lin Yang ◽  
Yuan Fang Li ◽  
Chun Mei Li ◽  
...  

The Analyst ◽  
2019 ◽  
Vol 144 (21) ◽  
pp. 6313-6320 ◽  
Author(s):  
Xi Chen ◽  
Ya Wang ◽  
Junjun Zhang ◽  
Yuzhong Zhang

A ultrasensitive electrochemical detection of prostate-specific antigen was reported based on hybridization chain reaction amplifying silver nanoparticles response signal.


RSC Advances ◽  
2015 ◽  
Vol 5 (55) ◽  
pp. 44714-44721 ◽  
Author(s):  
Siqi Zhang ◽  
Kun Wang ◽  
Zhenyu Li ◽  
Zhongmin Feng ◽  
Ting Sun

Upon adding THBV, the self-assembly of THBV with H1 allows the rest of the DNA sequence of H1 to accelerate H1–H2 complex formation. The G-quadruplex at the end of the H1–H2 complex could catalyze TMB into a colored product.


2016 ◽  
Vol 85 ◽  
pp. 128-134 ◽  
Author(s):  
Marta Garcia-Cortes ◽  
Jorge Ruiz Encinar ◽  
Jose M. Costa-Fernandez ◽  
Alfredo Sanz-Medel

1995 ◽  
Vol 41 (1) ◽  
pp. 54-58 ◽  
Author(s):  
H Yu ◽  
E P Diamandis

Abstract Prostate-specific antigen (PSA) is believed to be a highly specific marker for normal and cancerous prostatic tissue. We recently found that 30-40% of breast tumors produce PSA. Other data from our group suggest that normal breast can also produce PSA under conditions of stimulation by steroid hormones. In addition, we detected PSA in amniotic fluid. Here we report the presence of PSA in breast milk of lactating women. PSA concentrations in breast milk were quite variable, ranging from < 0.01 microgram/L in 4 of 38 milks to 350 micrograms/L; the median was 0.47 microgram/L. PSA concentration in breast milk was not correlated with mother's age or the sex of the newborn. It did tend to decrease with increasing time postdelivery, but was still detectable 2 weeks postdelivery. PSA in milk was equally measurable by a highly sensitive PSA assay based on time-resolved fluorometry and by the IMx automated PSA method. As confirmed by Western blot analysis, PSA in milk was present predominantly in its 33-kDa form; the PSA-alpha 1-antichymotrypsin complex (100 kDa) was also present but its concentration was < 25% of total PSA. We conclude that the female breast can produce PSA and that PSA is secreted into the milk during lactation; however, the biological role of PSA in milk is unknown. These and other data presented by our group suggest that PSA, a serine protease, may play a role in control of growth in mammary and other tissues through regulation of growth factors, cytokines, and growth-factor-binding proteins.


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