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Shazib Pervaiz

Publications and source records attributed to Shazib Pervaiz.

3 recordsLinked to original sources

A permissive apoptotic environment: function of a decrease in intracellular superoxide anion and cytosolic acidification.

Reactive oxygen species are involved in cellular processes as diverse as proliferation and cell death. At concentrations that do not overwhelm the cellular antioxidant defense systems, reactive oxygen species such as superoxide anion can inhibit death signaling. The sensitivity of cells to apoptotic triggers is significantly increased upon decreasing intracellular superoxide concentration. The critical determinant is the tight intracellular balance between superoxide and hydrogen peroxide levels, and a shift from the tightly regulated physiological ratio could impact cellular response to death stimuli. A shift toward hydrogen peroxide leads to activation of the effector components of the cells' apoptotic machinery by inducing reduction of the intracellular milieu and a drop in cytosolic pH, thereby creating a facilitative environment for efficient death execution. Hence, we propose that a permissive apoptotic milieu is a function of decreased intracellular superoxide concentration and cytosolic acidification.

Animals↗

Anti-cancer drugs of today and tomorrow: are we close to making the turn from treating to curing cancer?

Therapeutic management of cancer has undergone tremendous conceptual advance over the last couple of decades. Not only are we better acquainted with the intricate mechanisms leading to oncogenic transformation, but also the strategies to intercept and disturb these command and control pathways are becoming more specific and target-selective. One critical change is the realization that despite the existence of diverse mechanisms for the development of different sub-sets of cancers, there may indeed be central regulatory networks that serve as a common denominator in all forms of neoplasia. These critical events could endow cells with the potential for unabated proliferation, insensitivity to death inducing signals, and enhanced metastatic potential. Thus, developing strategies to target these critical events or pathways should significantly improve the outcome of cancer chemotherapy. The purpose of this review is to briefly discuss the complexities of the disease, highlight the current therapeutic strategies, and more importantly provide a mechanistic approach for future drug design aimed at targeting the traits of the disease and for favorably tailoring the response of cancer cells to drug therapy.

Antineoplastic Agents↗