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. Author manuscript; available in PMC: 2011 Feb 1.
Published in final edited form as: Peptides. 2009 Nov 26;31(2):284. doi: 10.1016/j.peptides.2009.11.013

Table 2.

Comparison of the ability of oGRP(1-46) and other activators of human bombesin receptors to stimulate phospholipase C activity in different human small cell lung cancer cell lines (SCLC).

Experimental/control
SCLC CELL NMB [D-Phe6, β-Ala11, Phe13, Nle14] Bn(6-14) GRP oGRP(1-46) oGRP(1-46) + GRPR or NMBR antagonist
(0.1 uM) (0.1 uM) (0.1 uM) (0.1 uM) (0.1 uM)
NCI-H69 1.03±0.06 1.31±0.04** 1.23±0.07* 1.10±0.02** 0.99±0.06
NCI-N417 1.01±0.06 3.14±0.34** 1.03±0.01 0.99±0.05 0.96±0.08
NCI-H209 1.25±0.11* 1.17±0.03** 1.11±0.04 1.17±0.04** 1.01±0.06
NCI-N592 1.08±0.06 1.05±0.04 1.03±0.04 1.01±0.04 1.05±0.02

The ability to activate phospholipase C and stimulate [3H]IP breakdown was determined for each of the Bn related peptides and oGRP(1-46), either alone or in the presence of a GRPR receptor antagonist ([(3-Ph-Pr6), His7, D-Ala11, D-Pro13, ψ (13–14), Phe14]Bn(6-14)NH2 [1 uM]) or a NMBR receptor antagonist (PD 168368)[1 uM]. Results are expressed as the experimental value divided by the control value. Results are means±SEM and are the average of at least 4 experiments.

*

p<0.05,

**

p<0.01 compared to no additions. Abbreviations (Jensen etal. 2008); SCLC, small cell lung cancer cells; β-Ala, β-alanine; Nle, norleucine; others -see Table 1 footnote.