Background and Objective: Modeling of glioma growth and evolution is of key importance for cancer diagnosis, predicting clinical progression and improving treatment outcomes of neurosurgery. However, existing models are unable to characterize spatial variations of the proliferation and infiltration of tumor cells, making it difficult to achieve accurate prediction of tumor growth. Methods: In this paper, a new growth model of brain tumor using a reaction-diffusion equation on brain magnetic resonance images is proposed. Both the heterogeneity of brain tissue and the density of tumor cells are used to estimate the proliferation and diffusion coefficients of brain tumor cells. The diffusion coefficient that characterizes tumor diffusion and infiltration is calculated based on the ratio of tissues (white and gray matter), while the proliferation coefficient is evaluated using the spatial gradient of tumor cells. In addition, a parameter space is constructed using inverse distance weighted interpolation to describe the spatial distribution of proliferation coefficient.Results: The glioma growth predicted by the proposed model were tested by comparing with the real magnetic resonance images of the patients. Experiments and simulation results show that the proposed method achieves accurate modeling of glioma growth. The interpolation-based growth model has higher average dice score of 0.0647 and 0.0545, and higher average Jaccard index of 0.0673 and 0.0573, respectively, compared to the uniform- and gradient-based growth models. Conclusions: The experimental results demonstrate the feasibility of calculating the proliferation and diffusion coefficients of the growth model based on patient-specific anatomy. The parameter space that characterizes spatial distribution of proliferation and diffusion coefficients is established and incorporated into the simulation of glioma growth. It enables to obtain patient-specific models about glioma growth by estimating and calibrating only a few model parameters.