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Цікавими є дані по переносу резисткнтного до цисплатина фенотипу при трансфекції генів v-src. Непухлинні епітеліальні клітини людини HAG-1 після трансфекції гену v-src набували неопластичного фенотипу та резистентності до цисплатина. У трансформованих клітинах спостерігали значне зменьшення формування міжланцюгових зшивок ДНК з їх послідовним швидким видаленням. Після обробки даних клітин інгібіторами src-кіназ знижувався рівень резистентності до цисплатина. Результати цієї роботи вказують на можливість участі продукту гена v-src в індукції резитентності до цисплатина шляхом модуляції деяких шляхів репарації ДНК [111].
Ампліфікація гена сорцина (кальцій-звязуючого білка з молекулярною масою 19-22кД) в деяких модельних системах асоціювалася з резистентним фенотипом [112]. Важко зараз сказати, чи є резистентність пов`язаною саме з сорцином чи разом з геном сорцина у клітинах ампліфіковані і інші, більш важливі для розвитку резистентності гени.
Таким чином резистентність до цисплатина має комплексний характер і пов`язана з рядом особливостей клітин на рівні цитоплазматичної мемрани, внутрішньоклітинних систем детоксикації, систем репарації та порушення функціональної активності генів p 53, bcl-2, fos, mdm 2, nm23та інших.
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