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These novel findings in breast cancer suggest that HDL may regulate various signaling pathways and may therefore alter tumor progression.
In addition, many PRRs have a number of other vital functions apart from participation in immune response realization: they may regulate various aspects of cell proliferation, survival, apoptosis, autophagy, reactive oxygen species generation, pyroptosis, angiogenesis, and, consequently, of tissue remodeling and repair.
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NAC proteins, which may also regulate various aspects of meristematic development like rhizome bud dormancy, are known to be expressed in monocot meristems [ 75] and to be regulated by auxin via a similar auxin-responsive ubiquitination process [ 76, 77].
The regulatory group includes genes encoding various TFs which can regulate various stress-inducible genes cooperatively or separately and may constitute gene networks.
This may indicate that these piRNAs are produced from their linked genes to regulate various PGC functions.
Lipids regulate various steps of endocytosis.
PIK3C3 is known to regulate various intracellular membrane trafficking events.
These small GTPases regulate various cellular signaling pathways [8], [9].
Proteins regulate various cellular processes.
MicroRNAs regulate various cell processes at the post-transcriptional level.
Thus, TGF-β and FGF-2 may cooperate with each other and may regulate EMT of various kinds of cells in cancer microenvironment during cancer progression.
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