QSAR studies of new pyrido[3,4-b]indole derivatives as inhibitors of colon and pancreatic cancer cell proliferation

Abstract

We have discovered a new class of pyrido[b]bindole derivatives that show potent and broad spectrum anticancer activity with IC50 values down to submicromolar levels. Structure–activity relationship data acquired with the compounds as antiproliferative agents against several cancer cell lines, i.e., human HCT116 colon cancer cell line, HPAC and Mia-PaCa2 pancreatic cancer cell lines, were subjected to two different QSAR modeling methods. A kernel-based partial least squares (KPLS) regression analysis with chemical 2D fingerprint descriptors, and a PHASE pharmacophore alignment with 3D-QSAR study. The KPLS method afforded successful predictive QSAR models for antiproliferative activity of the HCT116 colon cell line and on two of the pancreatic cancer cell lines HPAC and Mia-PaCa2, with the following statistics: R2s of 0.99, 0.99, and 0.98, for training set coefficients of determination, and external test set predictive r2s of 0.70, 0.58, and 0.70, respectively. The best 2D fingerprint descriptor for both the HCT116 and HPAC data out of the eight finger prints utilized was the atom triplet fingerprint; whereas the one that worked best for the Mia-PaCa2 data was the linear fingerprint descriptor. The PHASE pharmacophore based 3D-QSAR study afforded a four-point pharmacophore model comprising one hydrogen bond donor (D) and three ring (R) elements, which yielded a successful 3D-QSAR model only with the HCT116 cell line data with training set R2 of 0.683, and an external test set predictive r2 of 0.562. With the PHASE 3D-QSAR, the influence of electronic effects and hydrophobicity were visualized, and were in agreement with the observed SAR of substitutions, while the KPLS method the relative extent of contribution of each atom in a compound to the activity. These models will foster the lead optimization process for this potent series of anticancer pyrido [3,4-b]indole compounds.

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Acknowledgements

Financial support from the Colleges of Pharmacy at Rosalind Franklin University of Medicine and Science and the University of Tennessee Health Science Center is acknowledged, and so is financial support from National Institutes of Health (NIH)/ National Cancer Institute (NCI) grants CA100102 and RO1CA186662 subcontract (Zhang, PI) that partly supported the work in the Buolamwini laboratory. RZ was also supported by NIH/NCI grants R01 CA186662 and R01CA214019. The content is solely the responsibility of the authors, and does not necessarily represent the official views of the National Institutes of Health.

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Correspondence to John K. Buolamwini.

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JKB, RZ, and WW are co-inventors on patents pertaining to the compounds. The remaining authors declare that they have no conflict of interest.

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Deokar, H., Deokar, M., Wang, W. et al. QSAR studies of new pyrido[3,4-b]indole derivatives as inhibitors of colon and pancreatic cancer cell proliferation. Med Chem Res 27, 2466–2481 (2018). https://doi.org/10.1007/s00044-018-2250-5

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Keywords

  • KPLS
  • Fingerprints
  • 3D-QSAR
  • Anticancer activity
  • Beta-carboline
  • Pharmacophore