Method for determining cancer onset or cancer onset risk
A determination method, cancer technology, applied in disease diagnosis, material excitation analysis, nanotechnology for sensing, etc., can solve the problem of low detection sensitivity
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Embodiment 1
[0087] Preparation method of immunostained tissue sample
[0088] In order to distinguish the difference from Hercep Test (detection of breast cancer tissue by HER2 antibody), all Hercep Test-negative tissue samples were used as human breast cancer pathological tissue. On the other hand, there are cancer cases unrelated to the three main factors (ER, PgR, HER2) related to the proliferation of breast cancer. It is generally believed that the "triple negative" breast cancer has a poor prognosis and is difficult to treat. Here, "triple negative" breast cancer tissue samples are also discussed. Specifically, 4 test samples of breast cancer tissues from recurrent patients (relapse within about 1 year and death within 4 years) (one of the test samples was triple negative [because 20-25% of recurrent patients are "triple negative", so random Add the "triple negative" label to 1 of the 4 test samples]), "triple negative" breast cancer tissue from recurrent patients (recurrence within...
Embodiment 2
[0090] Problems with fluorescent immunohistostaining
[0091] For the immunostained tissue sample prepared in Example 1 above, a combination of a confocal unit (manufactured by Yokogawa Electric Corporation), a fluorescence microscope (manufactured by Olympus Corporation), and an electron multiplier CCD (EM-CCD) imaging device (Andor (manufactured by the company) was irradiated with excitation light at 488 nm, and then a fluorescence image (fluorescence still image) of quantum dot fluorescent particles (detected by PAR1ab-QD705) was obtained using a bandpass filter of 695 to 740 nm. figure 1 (b) shows an example of a fluorescence still image of a tissue sample of a patient with recurrent breast cancer. Autofluorescence is so strong that quantum dot fluorescent particles (detected by PAR1ab-QD705) cannot be detected at first glance. Actually, when comparing the fluorescence brightness of autofluorescence and quantum dot fluorescent particles (detected by PAR1-antibody), only a...
Embodiment 3
[0094] Creation of corrected fluorescence images with autofluorescence removed
[0095] Fluorescence still images with zero (0) fluorescence intensity of autofluorescence as background are required. In this way, the total fluorescence in the fluorescence still image can be calculated as the fluorescence derived from the quantum dot fluorescent particles. The contrast adjustment method of the above-mentioned embodiment 2 is a division method of fluorescence intensity, and zero (0) cannot be obtained by division, so it must be an image processing method using a subtraction method that can obtain zero (0). Thus, as an image processing method for removing autofluorescence in a fluorescent still image, the method described below is considered. First, the breast cancer tissue sample immunostained with quantum dot fluorescent particles is irradiated with excitation light (laser) with an excitation wavelength of 488 nm, and a fluorescence image of quantum dot fluorescent particles is...
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