Helicobacter pylori-possible role as biomarker for oral cancer

Oral cancer is the most common cancer diagnosed in Indian men and is the leading cause of cancer deaths. Amongst other causes infections with Helicobacter pylori is an emerging cause of oral squamous cell carcinoma. There is still confusion in the route of transmission and the exact etiopathogenesis of H. pylori associated oral cancer. Knowledge of the microbiology and immunology of H. pylori is important to prevent its spread and may be useful in identifying high-risk populations, especially in areas that have high rates of gastric lymphoma, gastric cancer, and gastric ulcer. This paper presents an overview of the important aspects of H. pylori

Evaluation of the effect of ultraviolet stabilizers on the change in color of pigmented silicone elastomer: An in vitro study

Aim and Objective: To compare and evaluate the effect of ultraviolet (UV) stabilizers (Chimassorb 81 and Uvinul 5050) on the color change of pigmented elastomer. Materials and Methods: Two pigments - Red (P112 Brilliant Red) and Yellow (P106 Yellow) and two UV stabilizers Chimassorb 81 and Uvinul 5050 were studied. A total of six groups of 10 samples each were fabricated using a combination of the above colors and stabilizers: Group A1 - Red control, Group A2 - Red + Chimassorb 81, Group A3 - Red + Uvinul 5050. Group B1 - Yellow control, Group B2 - Yellow + Chimassorb 81, Group B3 - Yellow + Uvinul 5050. All samples were subjected to ageing in an accelerated weathering chamber (Weather-Ometer). Color values L, a, and b were measured at 500 and 1000 h for all samples before and after weathering and change in color (Delta E) was calculated. Results: All groups showed a significant color change. At 500 h, Chimassorb 81 showed a statistically significant lesser change in both colors (red - 3.66 and yellow - 2.8) compared to their control groups (red - 5.19 and yellow - 4.9). At 1000 h, both UV stabilizers showed lesser color change (A2 - 5.49, B2 - 4.28, A3 - 7.47 and B3 - 4.09) as compared to their respective control groups (A1 - 9.57 and B1 - 5.91). Overall, the change in the color with Group A was more than Group B. Conclusion: Addition of UV stabilizers helped the reduction of color change. Chimassorb 81 showed a greater reduction in color change in both colors consistently at 500 and 1000 h

Assessment of collagen fiber nature, spatial distribution, hue and its correlation with invasion and metastasis in oral squamous cell carcinoma and surgical margins using Picro Sirius red and polarized microscope

Introduction: Oral squamous cell carcinoma (OSCC) comprises a bulk of all the oral malignancies and is posing a major health problem among the population. It is an established fact that tumor stroma plays a vital role in tumor progression. Therefore, methods to detect, quantify, and analyze collagen are of immense value in this regard. Picro Sirius red, which has the capability to detect thin fibers, although frequently used, is seldom exploited to the fullest extent. Aim: Our goal is not only to identify nature of fibers, but also to assess the fiber hue and the spatial distribution of different colors in various grades of OSCC and correlate it with the metastasis of the tumor. The study has also analyzed the nature of stromal elements along the clear, close and involved surgical margins of OSCC. Materials and Methods: Ten cases each of well, moderately and poorly differentiated OSCC as well as clear, close and involved margins were stained with haematoxylin eosin and picrosirius red staining for evaluation under polarized microscope. Results: In this study we found that the birefringence of the collagen fiber changed from orange red to yellowish green from well to poorly differentiated OSCC. The collagen fibers in well-differentiated carcinoma revealed polarizing colors of reddish orange around the tumor islands in the majority of the fields. To the best of our knowledge is not being studied so far in the English literature. Conclusion: In the present study, it has been observed that stromal changes at the invading front of the tumor islands and with increasing grade of the tumor can be evaluated more efficiently with the use of Picro Sirius red stain

The growth factors and cytokines of dental pulp mesenchymal stem cell secretome may potentially aid in oral cancer proliferation

Background: Growth factors and cytokines responsible for the regenerative potential of the dental pulp mesenchymal stem cell secretome (DPMSC-S) are implicated in oral carcinogenesis. The impact and effects of these secretory factors on cancer cells must be understood in order to ensure their safe application in cancer patients. Objective: We aimed to quantify the growth factors and cytokines in DPMSC-S and assess their effect on oral cancer cell proliferation. Materials and methods: DPMSCs were isolated from patients with healthy teeth (n = 5) that were indicated for extraction for orthodontic reasons. The cells were characterized using flow cytometry and conditioned medium (DPMSC-CM) was prepared. DPMSC-CM was subjected to a bead-based array to quantify the growth factors and cytokines that may affect oral carcinogenesis. The effect of DPMSC-CM (20%, 50%, 100%) on the proliferation of oral cancer cells (AW123516) was evaluated using a Ki-67-based assay at 48 h. AW13516 cultured in the standard growth medium acted as the control. Results: VEGF, HCF, Ang-2, TGF-α, EPO, SCF, FGF, and PDGF-BB were the growth factors with the highest levels in the DPMSC-CM. The highest measured pro-inflammatory cytokine was TNF-α, followed by CXCL8. The most prevalent anti-inflammatory cytokine in the DPMSC-CM was IL-10, followed by TGF-β1 and IL-4. Concentrations of 50% and 100% DPMSC-CM inhibited Ki-67 expression in AW13516, although the effect was non-significant. Moreover, 20% DPMSC-CM significantly increased Ki-67 expression compared to the control. Conclusions: The increased Ki-67 expression of oral cancer cells in response to 20% DPMSC-CM indicates the potential for cancer progression. Further research is needed to identify their effects on other carcinogenic properties, including apoptosis, stemness, migration, invasion, adhesion, and therapeutic resistance