Application of substances that induce irf8 expression in the preparation of drugs for treating liver cancer
A technology for the treatment of liver cancer, substances, applied in the field of medicine
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Embodiment 1
[0064] Example 1 Immunohistochemistry
[0065] Fresh prostate cancer and benign prostatic hyperplasia tissues were collected from Jiangsu Provincial Hospital of Traditional Chinese Medicine. After quick freezing in liquid nitrogen, paraffin sections were prepared. Prostate cancer tissue chips (HPro-Ade180PG-02, 180 points) were purchased from Shanghai Xinchao Company and commissioned for immunohistochemistry Detect the expression of IRF8, and invite senior pathologists to interpret the immunohistochemical results:
[0066] (1) Judgment of staining positive rate: First, observe the tissue point in the entire field of view under a low-magnification microscope, and then select 3 fields of view with different staining intensities for interpretation under a high-power microscope. Randomly record 100 cells in one field of view, and then record the percentage of positive cells in the 100 cells X1%. After looking at the percentages of positive cells in the other two fields of view, X2...
Embodiment 2
[0077] 2.1 DHT can up-regulate the expression of IRF8
[0078]As the ligand of AR, androgen plays a crucial role in the growth and malignant transformation of prostate cancer cells mediated by AR. Abnormal activation of the Androgen-AR signaling pathway is common in the development of prostate cancer. We found that with the increase of the pathological grade of prostate cancer, the expression of IRF8 increased, and the expression of IRF8 was positively correlated with the expression of AR. These studies suggest that there is a link between IRF8 and AR. Studies have shown that a group of ISG proteins in prostate cells can also be regulated by androgen as androgen-stimulated genes. In this example, we detected whether the expression of IRF8 was regulated by the AR signaling pathway. The AR-positive prostate cancer cell line LNCaP was pretreated with 5% carbon-adsorbed serum C-FBS for 24 hrs, and then stimulated with 10 nM DHT for 24 hrs to detect the expression of IRF8 by imm...
Embodiment 3
[0081] Example 3 LNCaP cells knock down IRF8 expression cell proliferation to accelerate
[0082] 3.1 Design and construction of IRF8 knockout cell lines LNCaP-shNC, LNCaP-shRNA1, LNCaP-shRNA2.
[0083] 3.1.1 Design of Oligo
[0084] DNA oligo was designed using Designer3.0 (Genepharma) software, and the primers were synthesized by Shanghai Gemma Pharmaceutical Technology Co., Ltd. The loop structure in the LV3-shRNA template uses TTCAAGAGA to avoid the formation of termination signals. The 5' end of the sense strand contains GATCC, which is complementary to the sticky end formed after BamHI digestion; the 5' end of the antisense strand contains AATTC, which is complementary to the sticky end formed after EcoRI digestion.
[0085] Sense strand: 5'-GATCC-(GN18)-(TTCAAGAGA)-(N18C)-TTTTTTG-3'
[0086] Antisense strand: 3'-G(CN18)-(AAGTTCTCT)-(N18G)-AAAAAACTTAA-5'
[0087] Table 3 Designed DNA Oligo
[0088]
[0089]
[0090] 3.1.2 Annealing of LV3-shDNA template
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