Review Article

Superparamagnetic Nanoparticles and RNAi-Mediated Gene Silencing: Evolving Class of Cancer Diagnostics and Therapeutics

Table 2

Development of siRNA in cancer therapy.

S. no. Cell LineTargetResultREF

(1) PC-3 and DU 145hTERTDownregulation of hTERT inhibited cell proliferation[27]
(2) HT144RRM2Downregulation of RRM2 inhibited cell proliferation[28]
(3) H1299 and MDA-MB-468Ran,TPX2, SCD1Reduced survival of human tumor cell lines[29]
(4) H1299PTTGDecreasing PTTG expression reduced tumor growth in vivo and in vitro [30]
(5) Panc-1, PCI-19, PAN-03-JCK, and so forthS100A4Knockdown of S100A4 suppressed cell growth, induced apoptosis, and decreased cell migration[31]
(6) MDA-MB-231 and ZR751uPADownregulation of decreased tumor invasion, angiogenesis, and growth[32]
(7) A549 and H460Nrf2Silencing inhibited tumor growth, and increasing efficacy of chemotherapy[33]
(8) Cx1, HCT8, HT29, HCT15, and so forth.CDCA1 and KNTC2Knockdown suppressed cell proliferation and induced apoptosis[34]
(9) A549 PC9Wild type p53 SurvivingInhibition of wildtype p53 upregulated antiapoptotic survin expression. Inhibition of surviving with mutated p53 depressed cell proliferation[35]
(10) Ten HNSCC cell lines from one nasal cavity cancer (RPMI12650)IGF2Upregulation acquired resistance for RDDP in human head and neck squamous cell carcinoma[36]