Tumorové markery
BCL-2 oncoprotein
- Associated with the development of androgen-independent prostate cancer
- High levels of expression in androgen-independent tumours in advanced stages of the pathology
- Upregulation of BCL-2
- After androgen ablation in prostate carcinoma cell lines
- In a castrated-male rat model
- Further established a connection between BCL-2 expression and prostate cancer progression [11]
Ki-67 expression
- By immunohistochemistry
- Significant predictor of patient outcome for men with prostate cancer [11]
PSMA
- Can serve as a marker or identifier for prostate cancer cells
Markery
Metabolity stanovované v diagnostickém panelu H NMR spectroscopy
- Sarcosine, cysteine, glutamate, asparagines, glycine, leucine, proline, threonine, histidine, n-acetyl-aspartic acid, inosine, inositol, adenosine, taurine, creatine, uric acid, glutathione, uracil, kynurenine, glycerol-s-phosphate, glycocholic acid, suberic acid, glutamic acid, xanthosine, 4-acetamidobutyric acid and thymine [1]
- Methyl histidine and proline
- In blood, serum, plasma as well as urine [1]
- Can be used to determine breast cancer, lung cancer, colon cancer and prostate cancer [1]
- Limited set gives a higher specificity and selectivity than the complete metabolome. [1]
- Methyl histidine and proline
- One or more from: acetate, citrate, isoleucine, leucine, tryptophane and lipids [1]
Moč PLS-DA analysis
- Only the integral segments of Methylhistidine and Proline
- Sensitivity of 100% and a specificity of 100%
- Changes in the different metabolites included in the panel
- Downregulation
- tryptophan, 1 -Methylhistidine, Proline, acetate [1]
- Upregulation
- Isoleucine and Leucine [1]
- Unchanged
- Citrate, oxoproline [1]
Literatura:
[1] Patent WO2011128256A1 - Metabolic markers for diagnosing of cancer - Patenty Google [Internet]. [citován 4. červen 2013]. Dostupné od: www.google.com/patents/WO2011128256A1?cl=en&hl=cs&dq=%2215454-75-8%22+OR+%225-oxoproline%22+OR+%22proline,+5-oxo-%22+OR+%225-Carboxy-2-pyrrolidinone%22+OR+%225-Oxo-2-pyrrolidincarbons%C3%A4ure%22+OR+%222-Pyrrolidone-5-carboxylic+acid+%22+OR+%225-OXO-2-PYRROLIDINECARBOXYLIC+ACID%22&source=udsIsentress (raltegravir)
- Can inhibit a virus linked to prostate cancer and chronic fatigue syndrome
- According to a press release from Emory University in Atlanta
- In 2006, xenotropic murine leukemia virus (XMRV) has been detected in some prostate cancer patients’ tumor biopsies
- Whittemore Peterson Institute in Nevada has suggested that XMRV is the causative agent of chronic fatigue syndrome in a majority of patients
- Singh led another recently published study demonstrating the presence of XMRV in 27 percent of prostate cancers examined
- Virus more likely to be found in the most-aggressive tumors
- XMRV may promote cancer by integrating into the host cell DNA and warping the cell’s ability to regulate its own genes.
- Both XMRV and HIV are retroviruses - similar traits and treatment approaches.
- Tested 45 approved and experimental ARVs and other antiviral compounds against XMRV in cell culture.
- The most potent drug against XMRV was Isentress
- Originally approved in 2007 for treatment-experienced patients.
- Three other compounds—another integrase inhibitor
- In addition to zidovudine (found in Retrovir, Combivir and Trizivir)
- And tenofovir (found in Viread, Truvada and Atripla),
- Two reverse transcriptase inhibitors—also inhibit XMRV replication.
- Could be used together in combination therapy, much like they’re used to treat HIV.
- None of the protease inhibitors stopped XMRV in test tube studies.
- Drugs inhibited XMRV at lower concentrations when two of them were used together
- www.poz.com/article/hiv-xmrv-raltegravir-18278-7136