2019
DOI: 10.1093/annonc/mdz452.032
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Regulatory interacting network between the immunomodulatory non-coding RNAs: miR-17-5p, MALAT1 and H19 lncRNAs in modulating the tumour microenvironment in TNBC

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Cited by 5 publications
(5 citation statements)
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“…This was supported by evidence that was reported by Li et al that MALAT-1 could directly sponge miR-34a in melanoma cells [54] and directly target miR-17–5p in macrophages [55] . Nonetheless, our group and others have recently proven the tumor suppressor effects of both miRNAs in TNBC cells [ 28 , 56 ] and their possible immunomodulatory role in several malignancies [ 57 , 58 ]. To confirm our hypothesis, expression profiling of the selected miRNAs was performed in the same cohort of BC patients recruited in the current study.…”
Section: Discussionmentioning
confidence: 99%
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“…This was supported by evidence that was reported by Li et al that MALAT-1 could directly sponge miR-34a in melanoma cells [54] and directly target miR-17–5p in macrophages [55] . Nonetheless, our group and others have recently proven the tumor suppressor effects of both miRNAs in TNBC cells [ 28 , 56 ] and their possible immunomodulatory role in several malignancies [ 57 , 58 ]. To confirm our hypothesis, expression profiling of the selected miRNAs was performed in the same cohort of BC patients recruited in the current study.…”
Section: Discussionmentioning
confidence: 99%
“…Such strategies represent a vicious evasion mechanism that obverts immune responses against tumors [15] . Another tactic that has been extensively studied by our research group is hijacking the immune-surveillance by TNBC tumors via genetic and epigenetic alterations which modulate several components of TME, consequently suppressing the infiltrating immune cellular activity [16] , [17] , [18] , [19] , [20] , [21] , [22] . Accordingly, re-sensitizing the cytotoxic immune cells at the TME through reversing these immunoediting processes is considered a milestone towards the development of more effective immunotherapeutic therapeutic modality.…”
Section: Introductionmentioning
confidence: 99%
“…Prostate cancer-associated 3 (PCA3) has, in particular, been approved by the FDA and is currently being sold as Progensa by Hologic Gen-Probe (Marlborough, MA, USA) for prostate cancer diagnosis [185]. Circulating ncRNAs such as PCA3 are more reliable than other CNAs due to their high stability in the bloodstream and resistance to nuclease-mediated fragmentation, as extensively studied and reviewed by our research group in [186][187][188][189][190][191]. Plasma lncRNAs, in particular, were reported to be less sensitive to degradation induced via repetitive freeze-thaw cycles, as well as prolonged exposure to 45 • C and room temperature [192].…”
Section: Hcc Immunotherapymentioning
confidence: 99%
“…Their interactions with microRNAs, mRNAs, proteins, and genomic DNA control their physiological and pathological roles. Transcribing long noncoding RNAs (LncRNAs) from loci connected to cancer has been proposed as a major contributor to cancer risk, since deregulation of gene expression is a key event in carcinogenesis [9].…”
Section: Introductionmentioning
confidence: 99%