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is pro-apoptotic.  If the ratio of Bcl-2 to BAX is great, then   hold considerable promise as therapeutic agents for HCC.
                        [78]
          apoptosis does not occur.  TARAP has downregulated the   Most of these studies are preclinical with very limited clinical
                               [73]
          expression of Bcl-2 and upregulated the expression of BAX,   data; therefore, the clinical efficacy of these products is still
          decreasing the Bcl-2-BAX ratio, hence inducing apoptosis.    far from being tested. There is a need to develop a dosing
                                                         [73]
          TARAP has been used in China for hepatitis and its use in HCC   from using the available technology to overcome the low
          needs further studies.                              bioavailability and to have a standard dosage for future
                                                              clinical trials. Once that is achieved, the safety of these
          LIVISTONA CHINENSIS SEED                            products in high doses needs to be ascertained, although
                                                              they have been in use for hundreds of years.
          L. chinensis seed has been used in China for cancer
                   [79]
                            [28]
          treatment.  Lin et al.  have evaluated the therapeutic role   Lack of good clinical trials testing these products compared
          of ethanol extract of the L. chinensis seed (EELC) against HCC   to sorafenib and other pharmacological therapy may be due
          both in vitro and in vivo. EELC has inhibited tumor growth   to lack of financial support to conduct such trails.
          in HCC xenograft mice and decreased the tumor weight by
          43%, moreover, EELC tumor inhibition was assessed in vitro   There is a pressing need for governmental funding and
          on HepG2 cells, and the maximum reduction in cell viability   collaboration between centers to conduct multicenter
          was around 60% in a maximum time of 24 h, it also induced   randomized open label studies using the standard of care,
                                                         [28]
          cell apoptosis in HCC xenograft mice and HepG2 cells.    with or without these products either individualized or in
          Moreover, EELC has induced the loss of the mitochondrion   combination.
          membrane potential in HepG2 cells, leading to apoptosis and
          stimulates the release of caspases 9 and 3 in HepG2 cells and   Financial support and sponsorship
          causes a rise in the BAX-Bcl-2 ratio, as what TARAP does. [28]  Nil.

          CROCIN                                              Confl ict of interest
                                                              There is no conflict of interest.
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                                                   [80]
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