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. 2020 Nov 26;21(23):8988. doi: 10.3390/ijms21238988

Table 3.

Antineoplastic activity of cyclitols in colon cancer.

Study Clinical Status Human/Animal Species Cyclitol Results
Shamsuddin et al. (1988) [48] AOM-induced colon cancer Rat IP6
  • Significant reduction of tumor incidence in the IP6-treated group

  • Significantly lower mitotic rate in the IP6-treated group

Shamsuddin et al. (1989) [56] AOM-induced colon cancer Rat IP6
  • Even though the treatment with IP6 was introduced five months after carcinogen administration, there was a significant reduction in the number of tumors and tumor volume, and a lower mitotic rate was observed

Baten et al. (1989) [50] DMH-induced colon cancer Mouse IP6
  • Significant increase in NK activity after IP6, Ins, and Ins + IP6 treatment

  • Increased NK activity was correlated with reduced tumor incidence

Ullah et al. (1990) [57] AOM-induced colon cancer Rat IP6
  • Supplementation with 1% IP6 in drinking water reduced tumor prevalence by 52.2%, frequency by 55.8%, and size by 62.3%

  • 0.1% IP6 significantly reduced tumor size (by 71%)

Pretlow et al. (1992) [49] AOM-induced colon cancer Rat IP6
  • Decreased incidence of tumors—25% in a group treated with IP6 versus 83% in a control group (p = 0.0045)

Yang et al. (1995) [52] HT-29 human colon carcinoma cells IP6
  • Statistically significant growth inhibition at 1 mM IP6 concentration and significant inhibition of DNA synthesis

  • Decreased level of proliferation marker PCNA after 48 h

Shivapurkar et al. (1995) [29] AOM-induced colon cancer Rat IP6
  • Significant reduction of colon tumor incidence at both 11 and 32 weeks of the experiment.

Challa et al. (1997) [58] AOM-induced colon cancer Rat IP6
  • IP6 significantly reduced the incidence of aberrant crypt foci

  • A synergy effect between IP6 and green tea was observed in reducing tumor multiplicity (especially with 2% of IP6 and 2% of green tea)

El-Sherbiny et al. (2001) [33] HT-29 human colon carcinoma cells IP6
  • Treatment with IP6 decreased S phase and arrest cells in the G0/G1 phase

  • Significant decrease in the percentage of Ki-67 expression in IP6-treated cells (p < 0.01)

Zhang et al. (2005) [51] DMH-induced colon cancer Rat IP6
  • Significant increase in blood NK activity in the IP6-treated group

  • Significant reduction in the multiplicity and size of tumors in the IP6-treated group

  • Significantly higher survival rate in the IP6-treated group

Liu et al. (2015) [53] HT-29 human colon carcinoma cells IP6
  • Significant inhibition of proliferation after exposure to IP6 (for 12 and 24 h)

  • Significant reduction of expression of PI3K, Akt, and pAkt in IP6-treated cells

  • Significant increase in the expression of caspase-9 in IP6-treated cells

Kapral et al. (2017) [54] Colon cancer Caco-2 cells IP6
  • Proliferation inhibition after 24 h incubation in 1–10 mM IP6 (p < 0.05); after 48 h incubation proliferation inhibition was statistically significant in 5–10 mM IP6

  • Higher apoptotic index in IP6-treated cells compared to the controls

  • Higher expression of p21Waf1/Cip1 and higher Caspase-3 activity in IP6-treated cells

  • Reduction of AKT-1 activity and p70S6K in IP6-treated cells

Schröterová et al. (2018) [55] Colon cancer SW620 cells IP6
  • Significant decrease in cell migration at all IP6 concentrations (dose-dependent)

  • Significant decrease in the levels of MMP-2 and MMP-9 after 12, 24, and 48 h exposure to all IP6 concentrations

  • Decreased level of I-Cam1 after 12 and 24 h exposure to 1 mM IP6 and decreased level of EpCam after 48 h exposure to 1 mM IP6, decreased level of N-cadherin after 12 and 48 h exposure to all IP6 concentrations