Background: Chronic inflammation and infections are associated with increased risk of prostate cancer development. detected [16]. The subgingival biofilm may induce a host release of pro-inflammatory mediators that elicit a chronic inflammatory response, leading to alveolar bone loss [10]. Furthermore, studies have indicated that oral health may influence systemic health [10]. Several reports showed an association between periodontal disease and systemic conditions such as cardiovascular disease [10], type 2 diabetes mellitus [10], preterm low birth weight infants [17-20], osteoporosis [10], rheumatoid arthritis [21,22], Parkinsons disease [23], Alzheimers disease [24], psoriasis [25], respiratory functions [26] and several types of human cancers [27]. In particular, individuals with periodontal disease have a greater risk of cancer overall and site-precise malignancies including oral [28], gastrointestinal [29], lung [9], pancreatic [30], hematologic [31] and prostate [8,9]. It has been reported that chronic inflammatory response to periodontal contamination impacts beyond the oral cavity [22] and might increase the risk of various malignancies [23-25]. This association is usually supported by the effectiveness of anti-inflammatory drugs in reducing the risk of oesophageal, gastric, colorectal, biliary, breast, pancreatic [21], and genitourinary cancers [26,27]. The aim of this review is usually to advance the hypothesis that periodontal diseases may be significant in its contribution to prostate inflammation and cancer. Materials and methods An electronic search was carried out in PubMed database until August 2018 for all those relevant publications that explored the association between periodontal diseases and/or periodontal microbes in prostate inflammation and malignancy. The following MeSH terms were used, Periodontal Disease [All Field], Prostate disease [MeSH terms], Prostate cancer [MeSH terms], Prostatic Inflammation [MeSH terms]. Literature published in the English language was included. Results and discussion Association between periodontal disease and prostate cancer Alloxazine A growing number of reports suggest that periodontal disease is usually significantly associated with an increased risk of prostate cancer [8,9]. Arora et al. (2010), in a prospective co-twin study, reported an association of prostate tumor and periodontal disease assessed by questionnaire-recorded teeth flexibility and prostate tumor (hazard proportion 1.47) [8]. In another analysis, Hujoel et al. (2003), within a potential cohort study, examined data from 11,328 people and Alloxazine confirmed a relationship between prostate tumor and periodontal disease (chances proportion 1.81) [9]. Regardless of the little test size of (20 situations) of prostate tumor, this research was the only person to include a primary evaluation from the periodontal condition and set up a positive association between both illnesses [9]. A scholarly research in Taiwan, by Hwang et al. (2014) demonstrated that periodontal treatment comprising scaling and main planing, subgingival curettage and periodontal flap medical procedures decreased the Alloxazine chance of tumor from the gastrointestinal system, lungs, human brain, and feminine reproductive organs [32]. Nevertheless, the chance of prostate and thyroid cancers was better even after periodontal treatment [32] significantly. Michaud and Hiraki (2008) reported an inverse association between your number of tooth lost and Alloxazine the chance of prostate tumor [31,33]. Nevertheless, the tooth loss isn’t representative of periodontal disease; Rabbit Polyclonal to C-RAF for instance, a person may get rid of tooth because of caries or fracture. Furthermore, in a more recent study it was found that periodontal disease was associated with a 14% higher risk of prostate cancer [34]. Overall, these studies indicate that, an association probably exists between periodontal diseases and prostate cancer, see Table 1. Joshi et al. (2010) from Case Western Reserve University evaluated serum prostate-specific antigen (PSA) levels as a marker of inflammation in patients with prostatitis and periodontitis and showed that subjects with both diseases have greater levels of PSA compared with either disease alone [35]. Furthermore, Alwithanani et al. (2015) reported the impact of treatment of periodontal disease on clinical symptoms of prostatitis showing that periodontal treatment improves.
Categories
- 11??-Hydroxysteroid Dehydrogenase
- 45
- 5-HT6 Receptors
- 7-TM Receptors
- 7-Transmembrane Receptors
- Acetylcholine Nicotinic Receptors, Non-selective
- Adrenergic ??1 Receptors
- Adrenergic Related Compounds
- AHR
- Aldosterone Receptors
- Androgen Receptors
- Antiprion
- AT2 Receptors
- ATPases/GTPases
- Atrial Natriuretic Peptide Receptors
- Calcineurin
- CAR
- Carboxypeptidase
- Casein Kinase 1
- Corticotropin-Releasing Factor
- CysLT1 Receptors
- Dardarin
- Deaminases
- Death Domain Receptor-Associated Adaptor Kinase
- Delta Opioid Receptors
- DMTs
- DNA-Dependent Protein Kinase
- Dual-Specificity Phosphatase
- Dynamin
- eNOS
- ER
- G Proteins (Small)
- GAL Receptors
- General
- GLT-1
- Glucagon and Related Receptors
- Glycine Receptors
- Growth Factor Receptors
- Growth Hormone Secretagog Receptor 1a
- GTPase
- Guanylyl Cyclase
- KDM
- Kinesin
- Lipid Metabolism
- Main
- MAPK
- MCH Receptors
- Muscarinic (M2) Receptors
- NaV Channels
- Neurotransmitter Transporters
- NFE2L2
- Nitric Oxide Precursors
- Nitric Oxide Signaling
- NPFF Receptors
- Opioid
- Other
- Other MAPK
- Other Peptide Receptors
- Other Transferases
- OX1 Receptors
- OX2 Receptors
- OXE Receptors
- PAO
- Phosphatases
- Phosphoinositide 3-Kinase
- Phosphorylases
- Pim Kinase
- Polymerases
- Purine Transporters
- Sec7
- Serine Protease
- Sodium/Calcium Exchanger
- Sphingosine Kinase
- V2 Receptors
-
Recent Posts
- [PubMed] [Google Scholar] 52
- Methods and Material 2
- It has been well established that harboring the allele enhances dementia associated with Alzheimers disease (AD), and several studies have supported a role of proteolysis as an important factor that may contribute to this risk [2,3C10]
- [PubMed] [Google Scholar]Xiao YF, Ke Q, Wang SY, Auktor K, Yang Con, Wang GK, Morgan JP, Leaf A
- Although passively-administered hyperimmune serum conferred protection in intact birds [15,17,18], the contribution of innate defenses and cell-mediated immunity to the control of APEC in the avian host remains ill-defined
Tags
- 68521-88-0
- a 105-120 kDa heavily O-glycosylated transmembrane glycoprotein expressed on hematopoietic progenitor cells
- Ankrd11
- Capn1
- Carboplatin cost
- DKFZp781B0869
- HA6116
- Hdac11
- IGF2R
- INK 128 supplier
- JTK4
- LRP2
- Masitinib manufacturer
- MDA1
- Mouse monoclonal to CD34.D34 reacts with CD34 molecule
- Mouse monoclonal to ERBB3
- Mouse monoclonal to INHA
- order NVP-AEW541
- PECAM1
- Rabbit Polyclonal to AML1
- Rabbit polyclonal to AML1.Core binding factor CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters.
- Rabbit Polyclonal to AQP12
- Rabbit Polyclonal to C-RAF phospho-Ser301)
- Rabbit Polyclonal to C-RAF phospho-Thr269)
- Rabbit polyclonal to CD80
- Rabbit Polyclonal to Claudin 3 phospho-Tyr219)
- Rabbit Polyclonal to CYSLTR1
- Rabbit polyclonal to DDX20
- Rabbit Polyclonal to EDG4
- Rabbit Polyclonal to FGFR2
- Rabbit Polyclonal to GAS1
- Rabbit Polyclonal to GRP94
- Rabbit polyclonal to INMT
- Rabbit Polyclonal to KAPCB
- Rabbit Polyclonal to MMP-2
- Rabbit Polyclonal to MT-ND5
- Rabbit Polyclonal to OR52E2
- Rabbit polyclonal to PHC2
- Rabbit Polyclonal to RAB31
- Rabbit Polyclonal to SLC25A31
- Rabbit Polyclonal to ZC3H13
- Rabbit polyclonal to ZNF268
- TNFRSF13C
- VAV1
- Vegfa