COMPOSITIONS DERIVED FROM GALENIA AFRICANA AND METHODS OF USE FOR CANCER TREATMENT

Information

  • Patent Application
  • 20190365840
  • Publication Number
    20190365840
  • Date Filed
    December 19, 2017
    6 years ago
  • Date Published
    December 05, 2019
    4 years ago
Abstract
The present invention discloses a cancer treatment method which includes the step of treating a patient having cancer with an extract from Galenia africana L. plant. The extract may include pinocembrin and/or 2′,4′ dihydroxychalcone and/or 7-hydroxyflavanone. The cancer may be breast cancer or melanoma. The composition may be solubilized with MPG and/or Suganate.
Description
FIELD OF INVENTION

The present invention relates to a cancer treatment method and composition.


More particularly, the present invention relates to a cancer treatment method and composition for treating breast cancer and melanoma.


BACKGROUND TO INVENTION

Kraalbos (KB) extracts from Galenia africana L. plant are known to be rich in pinocembrin, 2′,4′ dihydroxychalcone, 7-hydroxyflavanone and 2′,4′ dihydroxydihydrochalcone compounds. These molecules have previously been shown to exhibit varying degrees of cytotoxity on cancer cells.


It is an object of the invention to suggest a novel cancer treatment method and composition which includes an extract of Galenia africana.


SUMMARY OF INVENTION

According to the invention, a cancer treatment method includes the steps of treating a patient having cancer with an extract from Galenia africana L. plant.


Also according to the invention, a cancer treatment composition includes an extract from Galenia africana L. plant


The extract may include pinocembrin and/or 2′,4′ dihydroxychalcone and/or 7-hydroxyflavanone.


The cancer may be breast cancer.


The cancer may be melanoma.


The composition may be solubilized.


The composition may be solubilized with MPG and/or Suganate.







DETAILED DESCRIPTION OF INVENTION

The invention will now be described by way of example.


According to the invention, a cancer treatment method includes the steps of treating a patient having cancer with an extract from Galenia africana L. plant.


Also according to the invention, a cancer treatment composition includes an extract from Galenia africana L. plant


The extract may include pinocembrin and/or 2′,4′ dihydroxychalcone and/or 7-hydroxyflavanone.


The cancer may be breast cancer.


The cancer may be melanoma.


The composition may be solubilized.


The composition may be solubilized with MPG and/or Suganate.


Experiment 1

The objective of the experiment was to test the role of Galenia africana (GA) extracts on the proliferation of MCF-7 human breast cancer cells. Cells were treated with B1, B2, B3, D1, D1B2 or D1B3. D1 exhibited the most cytotoxicity (IC50 of 26.53 ug/ml), followed by B2 (IC50 of 32.28 ug/ml). Based on the chemical composition of these extracts, it is clear that those that contain high levels of 2′,4′ dihydroxychalcone have the most effect. Indeed, a combination of D1 and B3 at 50:50 ratio had minimal effect as compared to a combination of D1 and B2 at 70:30 ratio.


The results are shown below:









TABLE 1





IC50s of GA extracts on MCF-7 human breast cancer


cells


















B1
73.84 ug/ml



B2
46.68 ug/ml



D1
26.53 ug/ml



D1B2
32.28 ug/ml

















TABLE 2







Chemical compositions of GA extracts with emphasis on pinocembrin


and 2′,4′ dihydroxychalcone











Items, %
pinocembrin
2′,4′-dihydroxychalcone















B1
20.46
14.95



B2
40.86
42.97



B3
90.09
1.38



D1

75










Experiment 2

The objective of the experiment was to test the role of Galenia africana extracts on the proliferation of MCF-7 human breast cancer cells.


The results are shown below:












Chemical compositions of GA extracts














2′,4′-
2′,4′-


Batches
7-hydroxyflavanone
pinocembrin
dihydroxychalcone
dihydroxydihydrochalcone














LC0524(1)
3.3%
9.6%
7.6%
3.1%


LC0525(2)
3.0%
8.4%
6.8%
2.8%


LC0535(3)
2.4%
4.3%
3.4%
0.7%


Batch 4
2.4%
12.4%
8.9%
3.2%























Batches
IC50 value (ug/mL)



















LC0524(1)
146.0



LC0525(2)
93.39



LC0535(3)
195.6



Batch 4
148.1



Current
187.1




























IC50 value



Batches
(ug/mL)



















LC0524(1)
124.2



LC0525(2)
114



LC0535(3)
132



Batch 4
144.1



Batch 5
141.6




























IC50 value



Batches
(ug/mL)



















LC0524(1)
144.2



LC0525(2)
130.5



LC0535(3)
166.3



Batch 4
160.8



Batch 5
158.4










The following figure depicts ME1402 human melanoma cells treated with GA extracts after 48 hrs of incubation. Mean cell survival calculated as percentage of the mean vehicle control.


The following figure depicts MCF12A human breast cells treated with KB extracts after 48 hrs of incubation. Mean cell survival calculated as percentage of the mean vehicle control.

Claims
  • 1. A cancer treatment method which includes the step of treating a patient having cancer with an extract from Galenia africana L. plant.
  • 2. A method as claimed in claim 1, in which the extract includes pinocembrin and/or 2′,4′ dihydroxychalcone and/or 7-hydroxyflavanone.
  • 3. A method as claimed in claim 1, in which the cancer is breast cancer.
  • 4. A method as claimed in claim 1, in which the cancer is melanoma.
  • 5. A cancer treatment composition which includes an extract from Galenia africana L. plant.
  • 6. A composition as claimed in claim 5, in which the extract includes pinocembrin and/or 2′,4′ dihydroxychalcone and/or 7-hydroxyflavanone.
  • 7. A composition as claimed in claim 5, in which the cancer is breast cancer.
  • 8. A composition as claimed in claim 5, in which the cancer is melanoma.
  • 9. A composition as claimed in claim 5, which is solubilized.
  • 10. A composition as claimed in claim 9, in which the composition is solubilized with MPG and/or Suganate.
  • 11. (canceled)
  • 12. (canceled)
Priority Claims (1)
Number Date Country Kind
2016/08789 Dec 2016 ZA national
PCT Information
Filing Document Filing Date Country Kind
PCT/IB2017/058097 12/19/2017 WO 00