2020
DOI: 10.1016/j.bbrc.2020.03.064
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Downregulation of glypican-4 facilitates breast cancer progression by inducing cell migration and proliferation

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Cited by 24 publications
(17 citation statements)
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“…Together with the results from our survival analysis, we can conclude patients of those subtypes have a better prognosis with low levels of GPC4. Due to the partially contradicting results with the study by Munir et al ( 2020 ), we would encourage future research to look at this very relevant topic in more detail and to potentially investigate whether the presence or absence of hormone receptors has further effects on the capability of glypicans to perform their function.…”
Section: Discussionmentioning
confidence: 79%
See 1 more Smart Citation
“…Together with the results from our survival analysis, we can conclude patients of those subtypes have a better prognosis with low levels of GPC4. Due to the partially contradicting results with the study by Munir et al ( 2020 ), we would encourage future research to look at this very relevant topic in more detail and to potentially investigate whether the presence or absence of hormone receptors has further effects on the capability of glypicans to perform their function.…”
Section: Discussionmentioning
confidence: 79%
“…GPC4 is one of the lesser-studied members of the glypican family. A recent study by Munir et al suggested that downregulation of GPC4 could possibly increase cell migration, invasion and proliferative activities in breast cancer (Munir et al 2020 ). Interestingly, the authors showed that knock-down of GPC4 expression in MCF-7 cells using siRNA resulted in more migration activity of the cells.…”
Section: Discussionmentioning
confidence: 99%
“…Knockdown of glypican-4 was found to enhance cell motility, invasion, and growth of breast cancer cells. 25 Another glypican family member, glypican-6, appeared to play a critical role in enhancing invasive migratory potential of breast cancer cells. This was indirectly promoted by stimulation of Wnt5a expression, which in turn led to activation of p38 mitogen-activated protein kinase (MAPK) and Jun N-terminal kinase (JNK).…”
Section: Discussionmentioning
confidence: 99%
“…However, a significant reduction of cell surface tethered SDC1 and an increase of shed SDC1 in the ECM has been observed as a function of tumor progression and aggressiveness, suggesting the involvement of post-transcriptional mechanisms in SDC1 expression in this type of tumor. Differential regulation of SDC1 expression as well as of the other SDC isoforms, GPCs, and the other HSPGs has been found in several tumors ( Table 3 ) [ 105 , 106 , 107 , 108 , 109 , 110 , 111 , 112 , 113 , 114 , 115 , 116 , 117 , 118 , 119 , 120 , 121 , 122 , 123 , 124 , 125 , 126 , 127 , 128 , 129 , 130 , 131 , 132 , 133 , 134 , 135 , 136 , 137 , 138 , 139 , 140 , 141 , 142 , 143 , 144 , 145 , 146 , 147 , 148 , 149 , 150 , 151 , 152 , 153 ].…”
Section: Structural Features Biosynthesis and Enzymatic Modificamentioning
confidence: 99%