Effect and mechanism of long noncoding RNAs HOTAIR on occurrence and development of gastric cancer


In this study, we have a tendency to aimed toward searching for the long noncoding RNA (lncRNA) abnormally expressed in stomachic cancer (GC) tissues and analyzing the association of its expression level with the clinicopathological feature and patient prognosis. The biological operate of this lncRNA in incidence and development of GHz was studied in vivo and in vitro. The underlying molecular mechanism was any mentioned.


We investigated the lncRNA expression level in GHz tissues and traditional stomachic tissue layer tissues by lncRNA chips analysis. The expression of lncRNA HOTAIR was detected by quantitative real time enzyme chain reaction (qRT‐PCR). the connection between HOTAIR expression level and prognosis was investigated by analyzing clinical samples. The influence of HOTAIR downregulation on GHz cell proliferation, chemosensitivity, apoptosis, and invasion were determined by bromodeoxyuridine (BrdU) incorporation assay, flow cytometry analysis, and transwell assay. growth graft model was developed to check the influence of downregulated HOTAIR on tumor growth and metastasis.


lncRNA HOTAIR had a particularly high expression level in GHz cells, and expected poor prognosis in patients. Downregulation of HOTAIR might promote chemosensitivity, induce caspase-mediated cell death of GHz cells, and considerably inhibit GHz cell proliferation, invasion, and metastasis in vivo and in vitro.


It was established that HOTAIR vie a positive role in GHz incidence and development per the study in its mechanism, function, and clinical manifestation so it might be expected to become a replacement target in GHz interference and treatment. [1]

Personalizing Gastric Cancer Screening With Predictive Modeling of Disease Progression Biomarkers

Gastric cancer (GC) remains the third most typical reason behind cancer-related death worldwide. Infection with Helicobacter pylori is accountable for over seventieth of gigacycle per second incidence; settlement induces chronic inflammation, which might facilitate progression to internal organ metaplasia, dysplasia, and gigacycle per second (Correa pathway). Although H. pylori demolition may be a necessary beginning in gigacycle per second hindrance, some patients still get to advanced stage sickness if substantial tissue harm has occurred or inflammation persists. This progression is usually symptomless till cancer reaches stage IV, however economical, efficient screening protocols for patients United Nations agency gift with early stages of the Correa pathway don’t exist. Given the high interpatient nonuniformity in progression time through this pathway, such screening protocols should essentially be personalised. this needs the identification of reliable and longways assessable biomarkers of patient-specific progression. many viscus vegetative cell (GSC) markers as well as CD44, CD133, and Lgr5 are upregulated in gigacycle per second. Here we have a tendency to show a big stepwise increase in immunohistochemical staining for these markers in biopsies at totally different stages of the Correa pathway, suggesting GSC fraction to be a promising candidate biomarker for early detection of malignant transformation. we have a tendency to gift a mathematical model capable of each simulating clinically determined will increase in GSC fraction in longitudinal diagnostic assay samples of individual patients, and foretelling patient-specific sickness progression trajectories primarily based solely on characteristics known from assay at initial presentation. From these forecasts, personalised screening schedules could also be known that might enable early stratification of speculative patients, and probably earlier detection of abnormalcy or early-stage gigacycle per second. [2]

Serum Pepsinogen as a Predictor for Gastric Cancer Death


The purpose of this text is to validate the semipermanent association between initial humor enzyme (PG) measurements and ensuant internal organ cancer–specific deaths from a long-term longitudinal cohort.


Endoscopic police work are often effective and economical in reducing internal organ cancer mortality if a biomarker like humor PG is accessible to spot insecure people and if the biomarker is also specific to gastric cancer risk.


Between 1995 and 1998, a internal organ cancer–screening program was conducted during a insecure population: the primary stage concerned PG testing, and therefore the second stage concerned higher scrutiny. the result was internal organ cancer death, that was monitored till December 31, 2010; results were expressed because the hazard magnitude relation (HR) and corresponding ninety five confidence interval (CI) victimisation the Cox proportional hazards regression model. alternative causes of death were used as comparators.


Among participants (n=3514) aged ≥30 years, 1682 (47.9%) were screened to see humor PG levels. once sixteen years of follow-up, fourteen deaths from internal organ cancer were documented. variable analyses adjusted for age, sex, and Helicobacter pylori serologic positivism showed that PG-I [3]

FOXS1 is regulated by GLI1 and miR-125a-5p and promotes cell proliferation and EMT in gastric cancer

Gastric cancer (GC) is that the fourth most typical neoplasm and also the second leading explanation for cancer death. Identification of key molecular communication pathways concerned in stomachal carcinogenesis and progression facilitates early gigacycle per second diagnosing and also the development of targeted therapies for advanced gigacycle per second patients. rising proof has discovered an in depth correlation between forkhead box (FOX) proteins and cancer development. However, the prognostic significance of forkhead box S1 (FOXS1) in patients with gigacycle per second and also the operate of FOXS1 in gigacycle per second progression stay vague. during this study, we have a tendency to found that upregulation of FOXS1 was often detected in gigacycle per second tissues ANd powerfully related to with an aggressive composition and poor prognosis. useful assays confirmed that FOXS1 knockdown suppressed cell proliferation and colony numbers, with induction of cell arrest within the G0/G1 part of the cell cycle, whereas forced expression of FOXS1 had the alternative impact. in addition, forced expression of FOXS1 accelerated tumour growth in vivo and inflated cell migration and invasion through promoting epithelial–mesenchymal transition (EMT) each in vitro and in vivo. Mechanistically, the core promoter region of FOXS1 was known at nucleotides −660~ +1, and NFKB1 indirectly bind the motif on FOXS1 promoters and inhibit FOXS1 expression. sequence set enrichment analysis discovered that the FOXS1 gene was most profusely enriched within the hedgehog communication pathway which GLI1 expression was considerably related to with FOXS1 expression in gigacycle per second. GLI1 directly sure to the promoter motif of FOXS1 and considerably shrunken FOXS1 expression. Finally, we have a tendency to found that miR-125a-5p pent-up FOXS1 expression at the travel level by binding to the 3′ untranslated region (UTR) of FOXS1. Together, these results counsel that FOXS1 will promote gigacycle per second development and will be exploited as a diagnostic and prognostic biomarker for gigacycle per second. [4]

The Role of Metastatic Lymph Node Ratio in Gastric Cancer

Introduction: lymphatic tissue metastases at the stomachic cancer is that the one amongst the vital prognostic risk factors. during this study, we tend to measure the prognostic importance of the pathological process lymphatic tissue quantitative relation within the stomachic cancer cases.

Methods and Technique: during this study, we tend to enclosed fifty six stomachic carcinoma patient World Health Organization had curative surgery and evaluated retrospectively. Forty one amongst them were male (s.2) and fifteen (&.7) were feminine. applied math analysis of the results of this study was done by victimisation SPSS seventeen for Windows. Survey analysis was calculated with Kaplan-Meier take a look at and also the multivariant analysis was calculated with Cox proportional hazard model.

Results: In our study the factors that result the survey were the quantitative relation of range of the pathological process lymphatic tissue and also the cleft total lymph node (MLR-Metastatic lymphatic tissue Ratio), stage, range of the not concerned humor nodes, the diameter of neoplasm and differentiation of the tumor. The multivariant analysis showed that stage and also the MLR were the freelance prognostic factors.

Conclusion: MLO primarily based staging could be a straightforward, effective, and consistent technique for the evaluating the prognosis of the stomachic cancer patients World Health Organization had curative surgery and had concerned humor nodes. [5]


[1 ] Feng, X. and Huang, S., 2019. Effect and mechanism of long noncoding RNAs HOTAIR on occurrence and development of gastric cancer. Journal of cellular biochemistry, 120(5), pp.6899-6907. (Web Link)

[2] Walker, R., Mejia, J., Lee, J.K., Pimiento, J.M., Malafa, M., Giuliano, A.R., Coppola, D. and Enderling, H., 2019. Personalizing gastric cancer screening with predictive modeling of disease progression biomarkers. Applied Immunohistochemistry & Molecular Morphology, 27(4), pp.270-277. (Web Link)

[3] Chiang, T.H., Chiu, S.Y.H., Chen, S.L.S., Yen, A.M.F., Fann, J.C.Y., Liu, C.Y., Chou, C.K., Chiu, H.M., Shun, C.T., Wu, M.S. and Lin, J.T., 2019. Serum Pepsinogen as a Predictor for Gastric Cancer Death. Journal of clinical gastroenterology, 53(5), pp.e186-e193. (Web Link)

[4] FOXS1 is regulated by GLI1 and miR-125a-5p and promotes cell proliferation and EMT in gastric cancer

Sen Wang, Longke Ran, Wanfeng Zhang, Xue Leng, Kexin Wang, Geli Liu, Jing Song, Yujing Wang, Xianqin Zhang, Yitao Wang, Lian Zhang, Yan Ma, Kun Liu, Haiyu Li, Wei Zhang, Guijun Qin & Fangzhou Song Scientific Reportsvolume 9, Article number: 5281 (2019) (Web Link)

[5] Ekiz, İbrahim, Güldoğan, C., Gündoğdu, E., Kılıç, M. and Tez, M. (2018) “The Role of Metastatic Lymph Node Ratio in Gastric Cancer”, Journal of Advances in Medicine and Medical Research, 25(3), pp. 1-7. doi: 10.9734/JAMMR/2018/36954. (Web Link)


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