Skip to main content
. 2022 May 29;23(11):6108. doi: 10.3390/ijms23116108

Table 1.

ACPs showing antitumor and/or antiviral effects, classified according to their structural characteristics into four categories: α-helical, β-pleated sheets, random coil and cyclic [116,117].

Category Feature ACP Model
α-Helical
[118,119,120,121]
Peptides short in length
Simple in structure
Magainin II Lung cancer cells
(A549)
Aurein Glioblastoma cells
(T98G)
L-K6 Breast cancer cells
(MCF-7)
LL37 Colorectal cancer cells (HCT116)
FK-16
β-Pleated sheet
[122,123,124,125,126]
Two or more disulfide bonds Good stability
Structures more complex than α-helical
Bovine lactoferrin (LfcinB) Gastric cancer cells
(MGC803)
MPLfcinB6 Human T leukemia cells
MPLfcin-P13 Hepatocellular carcinoma cells (HepG2)
Human neutrophil peptide
(HNP-1)
Prostate cancer cells
(PC-3)
Random coil ACPs
[127,128,129,130,131]
Rich in proline and glycine
Lack of a typical secondary structure
Alloferon Herpes simplex virus
Human papillomavirus
KW-WK N.R.
PR39 N.R.
PR35 N.R.
Cyclic ACPs
[132,133,134]
Closed peptides composed of a head-to-tail cyclization backbone or disulfide bonds that form cystine knots
More stable than linear structures
Hedyotis diffusa Cytide 1–3 Prostate cancer cells
(PC3, DU145, LNCap)
H-10 Malignant melanoma cells (B16)
RA-XII Colorectal tumor cells (HCT116)

N.R. = not reported.